sither
APC (adenomatous polyposis coli)
LOVD v.3.0 Build 29 [
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Curator:
Instituto Nacional del Cancer
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Full data view for gene APC
The variants shown are described using the
NM_000038.5
NM_000038.6
NM_001127511.2
NM_001354895.2
transcript reference sequence.
Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Effect
: The variant's effect on the function of the gene/protein, displayed in the format 'R/C'. R is the value reported by the source (publication, submitter) and this classification may vary between records. C is the value concluded by the curator. Note that in some database the curator uses Summary records to give details on the classification of the variant.Values used: '+' indicating the variant affects function, '+?' probably affects function, '-' does not affect function, '-?' probably does not affect function, '?' effect unknown, '.' effect was not classified.
Exon
: Number of exon/intron containing variant; 2 = exon 2, 12i = intron 12, 2i_7i = exons 3 to 7, 8i_9 = border intron 8/exon 9.
DNA change (cDNA)
: Description of variant at DNA level, based on a coding DNA reference sequence (following HGVS recommendations); e.g. c.123C>T, c.123_145del, c.123_126dup.
RNA change
: Description of variant at RNA level (following HGVS recommendations).
r.123c>u
r.? = unknown
r.(?) = RNA not analysed but probably transcribed copy of DNA variant
r.spl? = RNA not analysed but variant probably affects splicing
r.(spl?) = RNA not analysed but variant may affect splicing
r.0? = change expected to abolish transcription
Protein
: Description of variant at protein level (following HGVS recommendations).
p.(Arg345Pro) = change predicted from DNA (RNA not analysed)
p.Arg345Pro = change derived from RNA analysis
p.? = unknown effect
p.0? = probably no protein produced
Zygosity
: Homozygous or Heterozygous
All options:
Homo
Hetero
Not specified
Co_ocurrence
: If the variant is present in co-ocurrence with a mutation, please select the name of the mutated gene. If not, please select "no".
All options:
no
N/A
BRCA1
BRCA2
CHEK2
FANCC
MLH1
MSH2
MSH6
MUTYH
PALB2
PMS2
PTEN
APC
TP53
STK11
TSC1
RET
VHL
PALB2
NBN
CDKN2A
LZTR1
ATM
ERCC5
NF1
SDHB
BARD1
NTHL1
FANCC
BLM
BRIP1
RAD51C
GJB2
G6PC
SMN1
Review status
: prueba
Allele
: On which allele is the variant located? Does not necessarily imply inheritance! 'Paternal' (confirmed or inferred), 'Maternal' (confirmed or inferred), 'Parent #1' or #2 for compound heterozygosity without having screened the parents, 'Unknown' for heterozygosity without having screened the parents, 'Both' for homozygozity.
DNA change (genomic) (hg38)
: Description of variant at DNA level, based on the genomic DNA reference sequence (following HGVS recommendations).
g.12345678C>T
g.12345678_12345890del
g.12345678_12345890dup
Reference
: Reference to publication describing the variant, including links to OMIM (when available), PubMed or or other source, e.g. "den Dunnen ASHG2003 P2346".
DB-ID
: Database ID of variant, grouping multiple observations of the same variant together, starting with the HGNC gene symbol, followed by an underscore (_) and a six digit number (e.g. DMD_012345). _000000 is used for variants where DNA was not analysed (change predicted from RNA analysis), variants seen in animal models or variants not seen in humans but functionally tested in vitro.
dbSNP ID
: The dbSNP ID.
Variant remarks
: Remarks regarding the variant described, e.g. germline mosaicism in mother, 345 kb deletion, muscle RNA analysed, not in 200 control chromosomes tested, on founder haplotype, etc.
Template
: Template(s) used to detect the sequence variant; DNA = genomic DNA, RNA = RNA (cDNA).
All options:
DNA
RNA = RNA (cDNA)
Protein
? = unknown
Technique
: Technique(s) used to identify the sequence variant.
All options:
? = Unknown
SEQ-NG = Next-Generation Sequencing
SEQ = SEQuencing
MLPA = Multiplex Ligation-dependent Probe Amplification
SEQ-NG-H = Next-Generation Sequencing - Helicos
SEQ-NG-I = Next-Generation Sequencing - Illumina/Solexa
SEQ-NG-R = Next-Generation Sequencing - Roche/454
SEQ-NG-S = Next-Generation Sequencing - SOLiD
arrayCGH = array for Comparative Genomic Hybridisation
arraySEQ = array for resequencing
arraySNP = array for SNP typing
arrayCNV = array for Copy Number Variation (SNP and CNV probes)
BESS = Base Excision Sequence Scanning
CMC = Chemical Mismatch Cleavage
CNV
CSCE = Conformation Sensitive Capillary Electrophoresis
DECoN = Detection of Exon Copy Number variants
DGGE = Denaturing-Gradient Gel-Electrophoresis
DHPLC = Denaturing High-Performance Liquid Chromatography
DOVAM = Detection Of Virtually All Mutations (SSCA variant)
ddF = dideoxy Fingerprinting
DSCA = Double-Strand DNA Conformation Analysis
EMC = Enzymatic Mismatch Cleavage
HD = HeteroDuplex analysis
MCA = high-resolution Melting Curve Analysis (hrMCA)
IHC = Immuno-Histo-Chemistry
MAPH = Multiplex Amplifiable Probe Hybridisation
Northern = Northern blotting
PCR = Polymerase Chain Reaction
PCRdig = PCR + restriction enzyme digestion
PCRlr = PCR, long-range
PCRm = PCR, multiplex
PCRq = PCR, quantitative
PAGE = Poly-Acrylamide Gel-Electrophoresis
PTT = Protein Truncation Test
PFGE = Pulsed-Field Gel-Electrophoresis (+Southern)
RT-PCR = Reverse Transcription and PCR
SBE = Single Base Extension
SSCA = Single-Strand DNA Conformation polymorphism Analysis (SSCP)
SSCAf = SSCA, fluorescent (SSCP)
Southern = Southern blotting
TaqMan = TaqMan assay
Western = Western Blotting
in-house algorithm for CNV
z-score-CNV = z-score based algorithm for CNV detection in targeted NGS
Date of test
: Date in which the results of the test were informed to the pacient
Lab
: Name of the Laboratory that performed the screening.
All options:
ARGENETICS
ARGENOMICS - Fundacion Investigar
Biocodices S.A.
Biogenotec
BIOMAKERS Molecular Pathology & Research
Bionet
Centro de Diagnostico Molecular (CDM)
Centro de Educación Médica e Investigaciones Clínicas (CEMIC)
Centro de Estudios Geneticos (CEG)
Centro de Investigaciones Endocrinologicas “Dr. Cesar Bergada” (CEDIE)
Centro Nacional de Genetica Medica "Dr. Eduardo E. Castilla" (CENAGEM)
Centro Privado Internacional de Medicina Personalizada - CEPIMP Genomics
CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS
CITOGEN.LAB
Clínica Universitaria Reina Fabiola
Dasa Genómica - Genia
Diagnus Lab
Domeq&Lafage
Fundacion BIOGEN
Fundación para el Progreso de la Medicina
FUNDAGEN S.A.
Gammalab - Grupo Gamma S.A.
GENDA
Genesia - Progenitest
Genologica laboratorio de análisis genéticos
GENOS
Grupo de investigacion en Genetica Aplicada (GIGA)
Hospital Alemán
Hospital de Alta Complejidad El Calafate - SAMIC
Hospital de Gastroenterología Dr. Carlos Bonorino Udaondo
Hospital Italiano de Buenos Aires
Hospital Privado Centro Médico de Córdoba
Hospital Universitario Austral
IACA Laboratorios
IBC Laboratorios
Instituto Alexander Fleming
Laboratorio Barros
Laboratorio de Biologia Celular y Molecular IHEM-CONICET CCT Mendoza
Laboratorio de Medicina Genomica - Facultad de Medicina - UNNE
Laboratorio Dr. Rapela
Laboratorio Dra. Marta Cortelezzi
Laboratorio Fares Taie
Laboratorio Flores
Laboratorio Hidalgo S.A.
Laboratorio High Medic Group S.A.
Laboratorio Integral SRL
Laboratorio Maipu
Laboratorio Motter
Laboratorio NANNI
Laboratorio PampaGEN
Laboratorio Tucumán
Laboratorios Turner
LACE Laboratorios
LEB (Laboratorio de Especialidades Bioquimicas)
MANLAB
MEDgenomica
PRICAI-Primer Centro Argentino de Inmunogenética-Fundación Favaloro
Sanatorio Allende
Stamboulian Laboratorio
STEM
VZ Laboratorios
Zoigen
AMBRY GENETICS
Baylor Genetics
Blueprint Genetics
CENTOGENE
COLOR
GENE ONE
Health in code
Iden Gene
IMEGEN
INVITAE
Laboratorio ATGen (E)
Laboratorio ATGen
MACROGEN
Myriad Genetics
SENTIS
Sistemas Genómicos
------
Color
Genda
Genda/Color
Genesia
Genesia/Invitae
Genia/Invitae
Genia/Color
Genia
Genos
Genos/Color
Hospital Privado Centro Médico de Córdoba
Hospital Privado Centro médico de Córdoba/IACA
Héritas
IACA
Invitae
AbaCid
Ambry Genetics
Alexander Fleming
Alexander Fleming/Baylor College
Alexander Fleming/Genesia-INVITAE
Argenomics
Baylor Genetics
BIOGEN
Biogenotec
BIOMAKERS Molecular Pathology & Research
BIONET
Blueprint Genetics
CEDIE
CEG
CEMIC
Centro de diagnóstico molecular
CEPIMP Genomics
CeNaGeM
Centogene
CIBIC
CIBIC/Héritas
Ciscato&Sharovsky
Clinica Universitaria Reina Fabiola
DIAGNUS LAB
Domeq&Lafage
Dr. Rapela
Fares Taie
FARESTAIE/Héritas
FAVALORO-PRICAI
Fundación para el Progreso de la Medicina
Fundación para el Progreso de la Medicina/CIBIC/Héritas
Fundagen
Gammalab
GeneDx
GIGA
Health in code
Hidalgo
High Medic Group
Hospital Alemán
Hospital de Gastroenterologia
Sanatorio Allende
MEDgenomica
LACE
HEMA
Centro médico de Córdoba
DASA-INVITAE
Bioscreen Rosario
x
Remarks
: Remarks
Type of test
: Type of test
All options:
Known familial mutation
Multigenetic panel
Specific pathology
Ashkenazi panel
Germline variant found in somatic testing
Whole exome
Ethnic origin
: The ethnic origin of the individual; e.g. African, Caucasian, gypsy, jew (Ashkenazi).
Reference
: Reference to publication describing the individual/family, possibly giving more phenotypic details than listed in this database entry, including link to PubMed or other source, e.g. "den Dunnen ASHG2003 P2346". References in the "Country:City" format indicate that the variant was submitted directly to this database by the laboratory indicated.
Remarks
: Remarks about the individual.
Cuadro familiar
: Principales canceres que motivan la sospecha clinica
How to query this table
All list views have search fields which can be used to search data. You can search for a complete word or you can search for a part of a search term. If you enclose two or more words in double quotes, LOVD will search for the combination of those words only exactly in the order you specify. Note that search terms are case-insensitive and that wildcards such as * are treated as normal text! For all options, like "and", "or", and "not" searches, or searching for prefixes or suffixes, see the table below.
Operator
Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
Arg Ser
all entries containing 'Arg' and 'Ser'
|
Text
Arg|Ser
all entries containing 'Arg' or 'Ser'
!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
=""
Text
="p.0"
all entries exactly matching 'p.0'
!=""
Text
!=""
all entries with this field not empty
!=""
Text
!="p.0"
all entries not exactly matching 'p.0?'
combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
all entries after June, 2020
>=
Date
>=2020-06-15
all entries on or after June 15th, 2020
combination
Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
>=
Numeric
>=23
all entries higher than, or equal to, 23
combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
Example
Matches
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
Asian|African !Caucasian
all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
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184 entries on 2 pages. Showing entries 1 - 100.
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Effect
Exon
DNA change (cDNA)
RNA change
Protein
Zygosity
Co_ocurrence
Review status
Allele
DNA change (genomic) (hg38)
Reference
DB-ID
dbSNP ID
Variant remarks
Template
Technique
Date of test
Lab
Remarks
Type of test
Disease
Ethnic origin
Reference
Remarks
Cuadro familiar
Panel size
Owner
-/-
5'UTR
c.-30257T>G
r.(=)
p.(=)
Hetero
no
RECLASSIFIED OCTOBER 2017
Unknown
g.112707687T>G
-
APC_000020
-
NM_001127511.2: c.-31T>G
DNA
SEQ-NG
15-mar-2017
CEMIC
-
-
-
Spanish
-
-
-
1
Alejandra Mampel-COIR
+/+
?
Deletion (Promoter 1B)
r.?
p.?
Hetero
N/A
-
Unknown
g.?
-
APC_000045
-
-
DNA
SEQ-NG
19-jul-2023
GENDA, INVITAE
Invitae Multi-cancer panel (84 genes)
Multigenetic panel
Polyposis
Spanish/Spanish
-
-
Polyposis
1
Maria Laura Gonzalez-Hospital Italiano
+/+
15-16
Exon 15-16 deletion
r.(?)
p.(?)
Hetero
N/A
-
Unknown
g.(?)
-
APC_000045
-
-
DNA
SEQ-NG
14-jun-2021
Invitae
Panel Invitae Multi-cáncer
Multigenetic panel
Colon cancer
Spanish
-
-
Colon cancer
1
Jesica Ramirez-Hospital Central de Mendoza
?/.
2
c.116C>A
r.(?)
p.(Thr39Asn)
Hetero
APC;DIS3L2
-
Unknown
g.112755006C>A
-
APC_000044
-
-
DNA
SEQ-NG
14-jun-2021
Invitae
Panel Invitae Multi-cáncer
Multigenetic panel
Colon cancer
Spanish
-
-
Colon cancer
1
Jesica Ramirez-Hospital Central de Mendoza
-/-
1i
c.136-53T>C
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112766273T>C
-
APC_000015
-
-
DNA
SEQ-NG
9-feb-2017
Genia
-
-
-
Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
1i
c.136-53T>C
r.(=)
p.(=)
Homo
no
-
Unknown
g.112766273T>C
-
APC_000015
-
-
DNA
SEQ-NG
9-may-2017
CEMIC
-
-
-
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
?/?
3
c.197T>C
r.(197u>c)
p.(Ile66Thr)
Hetero
no
-
Unknown
g.112766387T>C
-
APC_000063
-
-
DNA
SEQ-NG
05-07-21
Héritas
Panel (30 genes) APC, ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A (p14ARF), CDKN2A (p16INK4a), CHEK2, EPCAM, GREM1, MITF, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, POLE, POLD1, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53.
Multigenetic panel
N/A
Spanish/French-Argentinean
-
-
Breast cancer, Ovarian cancer
1
Laura Vargas Roig-IMBECU
-/-
3i
c.423-16A>T
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112775613A>T
-
APC_000017
-
-
DNA
SEQ-NG
15-mar-2017
CEMIC
-
-
-
Spanish
-
-
-
1
Alejandra Mampel-COIR
-/-
4i
c.423-4delA
r.?
p.?
Hetero
APC
-
Unknown
g.112775625delA
-
APC_000005
-
-
DNA
SEQ-NG, z-score-CNV
3-may-2017
Héritas
-
-
-
European
-
-
-
1
Alejandra Mampel-Hospital Universitario de Mendoza
+/+
5
c.509_512del
r.(509_512del)
p.(Asp170Valfs*4)
Hetero
N/A
-
Unknown
g.112775715_112775718del
-
APC_000060
-
-
DNA
SEQ-NG
20-feb-2022
Genda/Color
Hereditary Cancer Test (30 genes) APC, ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A (p14ARF), CDKN2A (p16INK4a), CHEK2, EPCAM, GREM1, MITF, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53
Multigenetic panel
Colon cancer
Italian
-
-
Colon cancer
1
Jesica Ramirez-Hospital Central de Mendoza
+/+
5
c.509_512delATAG
r.(?)
p.(Asp170Valfs*4)
Hetero
N/A
-
Unknown
g.112775715_112775718delATAG
-
APC_000012
-
-
DNA
SEQ-NG, z-score-CNV
3-may-2017
Héritas
-
-
-
European
-
-
-
1
Alejandra Mampel-Hospital Universitario de Mendoza
+/+
4i
c.532-1G>A
r.spl?
p.?
Hetero
N/A
-
Unknown
g.112780789G>A
-
APC_000050
-
-
DNA
SEQ-NG
07-feb-2019
Myriad
NGS de APC y MUTYH
Specific pathology
-
German
-
-
-
1
Marcela Lopez - Instituto Donna
+/+?
6
c.574G>T
r.(574g>u)
p.(Glu192*)
Hetero
N/A
-
Unknown
g.112780832G>T
-
APC_000059
-
-
DNA
SEQ-NG
31-may-2022
Genda/Color
Hereditary Cancer Test (30 genes) APC, ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A (p14ARF), CDKN2A (p16INK4a), CHEK2, EPCAM, GREM1, MITF, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53
Multigenetic panel
--
Unknown
-
-
-
1
Claudia Martin-Hospital de Córdoba
-?/-
5
c.607C>G
r.(?)
p.(Gln203Glu)
Hetero
no
RECLASSIFIED JULY 2022
Unknown
g.112780865C>G
-
APC_000028
-
-
DNA
SEQ-NG
22-oct-2018
Héritas
Panel Héritas (25 genes) APC,ATM,BMPR1A,BRCA1,BRCA2,BRIP1,CDH1,CDK4,CDKN2A,CHEK2,MLH1,MSH2,MSH6,MUTYH,PMS2,NBN,NF1,PALB2,PTEN,RAD51C,RAD51D,SMAD4,STK11,TP53,EPCAM
Multigenetic panel
--
Italian-German
-
-
-
1
Laura Vargas Roig-IMBECU
?/?
7
c.772G>A
r.(?)
p.(Glu258Lys)
Hetero
no
-
Unknown
g.112801321G>A
-
APC_000053
-
-
DNA
SEQ-NG
28-sep-2020
LACE
", Panel (30 genes) APC, ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EPCAM, GREM1, MITF, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53.",
Multigenetic panel
--
Spanish; Italian
-
-
-
1
Cecilia Montes-IMGO
?/?
9
c.905G>A
r.(?)
p.(Arg302Gln)
Hetero
no
-
Unknown
g.112815565G>A
-
APC_000038
-
-
DNA
CNV, SEQ-NG
14-nov-2019
Color (deriv. Genos)
Panel (APC, ATM, BAP1, BMPR1A, BRIP1, BRCA1, BRCA2, CDH1, CDK4, CDKN2A (p14ARF), CDKN2A (p16INK4a), CHEK2, EPCAM, GREM1, MITF, MLH1, MSH2, MSH6, NBN, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53)
Multigenetic panel
-
Spanish
-
(antec. personales/NO explica cuadro personal)
-
1
Pablo Kalfayan-Hospital Italiano
?/?
9
c.905G>A
r.(?)
p.(Arg302Gln)
Hetero
no
-
Unknown
g.112815565G>A
-
APC_000038
-
-
DNA
CNV, SEQ-NG
30-apr-2019
Color (deriv. Genda)
Hereditary Cancer Risk Test (30 genes)
Multigenetic panel
-
Paraguayan-Argentinian
-
-
-
1
Yolanda Medina-Hospital de la Madre y el Niño
+/+?
10
c.961dup
r.(961dup)
p.(Met321Asnfs*6)
Hetero
no
-
Unknown
g.112818993dup
-
APC_000064
-
-
DNA
SEQ-NG
03-02-22
Hospital Universitario Austral
Panel (30 genes) APC, ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EPCAM, GREM1, MITF, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, POLE, POLD1, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53.
Multigenetic panel
Colonic Polyposis
Spanish/Spanish
-
-
Colonic Polyposis
1
Maria Laura Gonzalez-Hospital Italiano
+/+
10
c.994C>T
r.(?)
p.(Arg332*)
Hetero
N/A
-
Unknown
g.112819026C>T
-
APC_000031
-
-
DNA
SEQ-NG, CNV
15-aug-2019
GENDA, COLOR
Hereditary Cancer Risk Test (30 Genes)
Multigenetic panel
-
Spanish
-
CII (explica cuadro)
-
1
Pablo Kalfayan-Hospital Italiano
?/?
10
c.1283A>G
r.(?)
p.(Glu428Gly)
Hetero
no
-
Unknown
g.112819315A>G
-
APC_000039
-
-
DNA
CNV, SEQ-NG
20-jul-2019
Invitae (deriv. Genesia)
Invitae Multi-Cancer Panel (84 genes)
Multigenetic panel
Breast cancer
Italian
-
-
Breast cancer
1
Jesica Ramirez-Hospital Central de Mendoza
-/-
11
c.1458T>C
r.(=)
p.(=)
Hetero
APC
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
SEQ-NG, z-score-CNV
3-may-2017
Héritas
-
-
-
European
-
-
-
1
Alejandra Mampel-Hospital Universitario de Mendoza
-/-
11
c.1458T>C
r.(=)
p.(=)
Homo
no
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
SEQ-NG
4-jul-2016
CEMIC
-
-
Healthy/Control
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
11
c.1458T>C
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
SEQ-NG
15-mar-2017
CEMIC
-
-
-
Spanish
-
-
-
1
Alejandra Mampel-COIR
-/-
11
c.1458T>C
r.(=)
p.(=)
Homo
no
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
SEQ-NG
22-mar-2017
CEMIC
-
-
-
Spanish
-
-
-
1
Pablo Kalfayan-CEMIC
-/-
11
c.1458T>C
r.(=)
p.(=)
Homo
APC
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
SEQ-NG
6-sep-2017
Genia
-
-
-
Spanish
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
11
c.1458T>C
r.(=)
p.(=)
Homo
APC
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
SEQ-NG
5-dec-2018
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
-
Italian
-
CIA (antec personales/explica cuadro)
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
11
c.1458T>C
r.(=)
p.(=)
Hetero
MUTYH
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
SEQ-NG
16-apr-2019
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
-
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
11
c.1458T>C
r.(=)
p.(=)
Homo
no
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
SEQ-NG
3-abr-2019
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
--
Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
11
c.1458T>C
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
CNV, SEQ-NG
28-mar-2018
IACA
Panel (APC, ATM, BMPR1A, BRCA1, BRCA2, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, SMAD4, STK11, TP53)
Multigenetic panel
Breast cancer
Argentinian
-
-
Breast cancer, Colon cancer
1
Silvina Sisterna-Hospital de Comunidad
-/-
12
c.1458T>C
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112827157T>C
-
APC_000006
rs2229992
APC(NM_001127511.3):c.1458T>C p.(Ala486=)
DNA
CNV, SEQ-NG
16-aug-2019
IACA
Panel (APC, ATM, BMPR1A, BRCA1, BRCA2, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, SMAD4, STK11, TP53, VHL)
Multigenetic panel
Breast cancer, Kidney cancer
Spanish-Italian
-
-
Breast cancer, Kidney cancer
1
Silvina Sisterna-Hospital de Comunidad
-/-
11
c.1458T>C
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
SEQ-NG
22-nov-2019
Biogenotec
Panel (APC, ATM, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, MLH1, MSH2, MSH6, MUTYH, NBN, NF1, PALB2, PMS2, PTEN, RAD51D, RAD51D, SMAD4, STK11, TP53, EPCAM)
Multigenetic panel
-
Unknown
-
-
-
1
Laura Vargas Roig-IMBECU
-/-
11
c.1458T>C
r.(=)
p.(=)
Homo
no
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
SEQ-NG
24-aug-2020
CEMIC
-
Specific pathology
--
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
11
c.1458T>C
r.(=)
p.(=)
Homo
no
-
Unknown
g.112827157T>C
-
APC_000006
-
-
DNA
CNV, SEQ-NG
27-nov-2019
Invitae
(deriv. Genesia) Invitae Multi-Cancer Panel (84 genes)
Multigenetic panel
Colon cancer
Spanish-Italian
-
-
Colon cancer
1
Lina Nuñez-Private Practice
?/?
13
c.1580G>C
r.(1337g>a)
p.Arg527Thr
Hetero
no
-
Unknown
g.112827960G>C
-
APC_000071
rs1554081889
-
DNA
SEQ-NG
26-01-22
CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS
Hereditary Colorectal Cancer Panel (22 Genes) APC, ATM, BLM, BMPR1A, CDH1, CHEK2, EPCAM, GALNT12, GREM1, MLH1, MSH2, MSH3, MSH6, MUTYH, NTHL1, PMS2, POLD1, POLE, PTEN, SMAD4, STK11, TP53.
Multigenetic panel
Colon cancer
Paraguaian - Argentinean
-
-
Colon cancer
1
Yolanda Isabel Medina - Hospital Juan D. Perón
?/?
13
c.1621C>A
r.(?)
p.(Gln541Lys)
Hetero
no
-
Unknown
g.112828001C>A
-
APC_000046
-
-
DNA
SEQ-NG
04-dec-2020
Fares Taie
Panel (56 genes) APC, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, DICE1, FANCC, FANCM, FH, FLCN, GALNT12, HOXB13, KIT, MEN1, MET, MITF, MLH1, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NF2, NYHL1, PALB2, PMS2, POLD1, POLE, PTEN, RAD50, RAD51C, RAD51D, RB1, RECQL4, RET, RINT1, SDHA, SDHB, SDHC, SDHD, SMAD4, SMARCA4, STK11, TP53, TSC1, TSC2, VHL, XRCC2.
Multigenetic panel
N/A
Italian; Spanish
-
-
Colon cancer
1
Silvina Sisterna-Hospital de Comunidad
-/-
13
c.1635G>A
r.(=)
p.(=)
Hetero
APC
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG, z-score-CNV
3-may-2017
Héritas
-
-
-
European
-
-
-
1
Alejandra Mampel-Hospital Universitario de Mendoza
-/-
13
c.1635G>A
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
9-feb-2017
Genia
-
-
-
Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
13
c.1635G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
4-jul-2016
CEMIC
-
-
Healthy/Control
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
13
c.1635G>A
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
15-mar-2017
CEMIC
-
-
-
Spanish
-
-
-
1
Alejandra Mampel-COIR
-/-
13
c.1635G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
22-mar-2017
CEMIC
-
-
-
Spanish
-
-
-
1
Pablo Kalfayan-CEMIC
-/-
13
c.1635G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
9-may-2017
CEMIC
-
-
-
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
13
c.1635G>A
r.(=)
p.(=)
Homo
APC
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
6-sep-2017
Genia
-
-
-
Spanish
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
13
c.1635G>A
r.(=)
p.(=)
Homo
APC
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
5-dec-2018
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
-
Italian
-
CIA (antec personales/explica cuadro)
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
13
c.1635G>A
r.(=)
p.(=)
Hetero
MUTYH
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
16-apr-2019
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
-
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
13
c.1635G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
22-mar-2019
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
--
Spanish
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
13
c.1635G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
3-abr-2019
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
--
Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
13
c.1635G>A
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
CNV, SEQ-NG
28-mar-2018
IACA
Panel (APC, ATM, BMPR1A, BRCA1, BRCA2, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, SMAD4, STK11, TP53)
Multigenetic panel
Breast cancer
Argentinian
-
-
Breast cancer, Colon cancer
1
Silvina Sisterna-Hospital de Comunidad
-/-
14
c.1635G>A
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112828864G>A
-
APC_000007
rs351771
NM_001127510.3 c.1635G>A p.(Ala545=)
DNA
CNV, SEQ-NG
16-aug-2019
IACA
Panel (APC, ATM, BMPR1A, BRCA1, BRCA2, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, SMAD4, STK11, TP53, VHL)
Multigenetic panel
Breast cancer, Kidney cancer
Spanish-Italian
-
-
Breast cancer, Kidney cancer
1
Silvina Sisterna-Hospital de Comunidad
-/-
13
c.1635G>A
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
22-nov-2019
Biogenotec
Panel (APC, ATM, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, MLH1, MSH2, MSH6, MUTYH, NBN, NF1, PALB2, PMS2, PTEN, RAD51D, RAD51D, SMAD4, STK11, TP53, EPCAM)
Multigenetic panel
-
Unknown
-
-
-
1
Laura Vargas Roig-IMBECU
-/-
13
c.1635G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
SEQ-NG
24-aug-2020
CEMIC
-
Specific pathology
--
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
13
c.1635G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112828864G>A
-
APC_000007
-
-
DNA
CNV, SEQ-NG
27-nov-2019
Invitae
(deriv. Genesia) Invitae Multi-Cancer Panel (84 genes)
Multigenetic panel
Colon cancer
Spanish-Italian
-
-
Colon cancer
1
Lina Nuñez-Private Practice
-/-
14i
c.1958+8T>C
r.(=)
p.(=)
Hetero
no
RECLASSIFIED JUNE 2019
Unknown
g.112835173T>C
-
APC_000018
-
-
DNA
SEQ-NG
15-mar-2017
CEMIC
-
-
-
Spanish
-
-
-
1
Alejandra Mampel-COIR
?/?
16
c.1994T>C
r.(1994u>c)
p.(Leu665Ser)
Unknown
no
-
Unknown
g.112837588T>C
-
APC_000066
-
Possible mosaicism
DNA
SEQ-NG
17-11-22
LACE
Hereditary extended cancer panel (84 GENES) AIP, ALK, APC*, ATM*, AXIN2, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CASR, CDC73, CDH1, CDK4, CDKN1B, CDKN1C, CDKN2A (p14ARF), CDKN2A (p16INK4a), CEBPA, CHEK2, CTNNA1, DICER1*, DIS3L2, EGFR, EPCAM*, FH*, FLCN, GATA2, GPC3*, GREM1*, HOXB13, HRAS, KIT, MAX*, MEN1*, MET*, MITF*, MLH1*, MSH2*, MSH3*, MSH6*, MUTYH, NBN, NF1*, NF2, NTHL1, PALB2, PDGFRA, PHOX2B*, PMS2*, POLD1*, POLE, POT1, PRKAR1A, PTCH1, PTEN*, RAD50, RAD51C, RAD51D, RB1*, RECQL4*, RET, RUNX1, SDHA*, SDHAF2, SDHB, SDHC*, SDHD, SMAD4, SMARCA4, SMARCB1, SMARCE1, STK11, SUFU, TERC, TERT, TMEM127, TP53, TSC1*, TSC2, VHL, WRN*, WT1 .
Multigenetic panel
Thyroid cancer
Basque/Italian
-
-
Thyroid cancer
1
Claudia Martin-Hospital de Córdoba
+/+
15
c.1994T>G
r.(?)
p.(Leu665*)
Hetero
MUTYH
-
Unknown
g.112837588T>G
-
APC_000035
-
-
DNA
SEQ-NG, CNV
14-oct-2019
Genesia - Progenitest, INVITAE
Invitae Multi-Cancer Panel (84 genes)
Multigenetic panel
Colon cancer
Spanish
-
(antec ambos/explica cuadro)
Colon cancer
1
Jesica Ramirez-Hospital Central de Mendoza
+/+?
15
c.2385_2386delCT
r.(?)
p.(Tyr796Trpfs*2)
Hetero
no
-
Unknown
g.112837979_112837980delCT
-
APC_000051
-
-
DNA
SEQ-NG
23-mar-2019
CIBIC/Héritas
Panel cáncer de colon hereditario Héritas (14 genes) APC,ATM,BMPR1A,CHEK2, EPCAM,MLH1,MSH2,MSH6,MUTYH,PMS2,PTEN,SMAD4,STK11,TP53
Multigenetic panel
-
German
-
-
-
1
Marcela Lopez-CEMAFE
+/+?
15
c.2520dup
r.(?)
p.(Asp842Argfs*2)
Hetero
N/A
RECLASSIFIED JULY 2022
Unknown
g.112838114dup
-
APC_000022
-
-
DNA
SEQ-NG
6-sep-2017
Genia
-
-
-
Spanish
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
?/?
15
c.2995C>G
r.(?)
p.(Gln999Glu)
Hetero
no
-
Unknown
g.112838589C>G
-
APC_000049
-
-
DNA
SEQ-NG
28-oct-2020
Genos
Panel (16 genes) APC, AXIN2, BMPR1A, CHEK2, EPCAM, GREM1, MLH1, MSH2, MSH6, MUTYH, NTHL1, PMS2, PTEN, POLE, POLD1, SMAD4, STK11, TP53
Multigenetic panel
-
Spanish; Unknown
-
-
-
1
Pablo Kalfayan-Hospital Italiano
+/+
15
c.3183_3187del
r.(?)
p.(Gln1062*)
Hetero
N/A
-
Unknown
g.112838777_112838781del
-
APC_000033
-
-
DNA
SEQ-NG
5-dec-2018
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
-
Italian
-
CIA (antec personales/explica cuadro)
-
1
Maria Laura Gonzalez-Hospital Italiano
?/?
16
c.3193C>A
r.(3193c>a)
p.(Gln1065Lys)
Hetero
no
-
Unknown
g.112838787C>A
-
APC_000055
-
-
DNA
SEQ-NG
13-sep-2021
Genos/Color
Panel GENOS (30 genes) APC, ATM, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EPCAM, FLCN, GREM1, MLH1, MSH2, MSH6, MUTYH, NBN, NTHL1, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53
Multigenetic panel
-
Paraguayan-Paraguayan
-
-
-
1
Pablo Kalfayan-Hospital Italiano
?/-
15
c.3386T>C
r.(?)
p.(Leu1129Ser)
Hetero
no
-
Unknown
g.112838980T>C
-
APC_000037
-
-
DNA
CNV, SEQ-NG
25-jul-2018
Héritas
Panel (APC,ATM,BMPR1A,BRCA1,BRCA2,BRIP1,CDH1,CDK4,CDKN2A,CHEK2,EPCAM,MLH1,MSH2,MSH6,MUTYH,NBN,NF1,PALB2,PMS2,PTEN,RAD51C,RAD51D,SMAD4,STK11,TP53)
Multigenetic panel
-
Spanish
-
-
-
1
Laura Vargas Roig-IMBECU
?/?
16
c.3629A>T
r.(3629a>u)
p.(His1210Leu)
Hetero
no
-
Unknown
g.112839223A>T
-
APC_000061
-
-
DNA
SEQ-NG
24-jun-2022
Genda/Color
Hereditary Cancer Test (30 genes) APC, ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A (p14ARF), CDKN2A (p16INK4a), CHEK2, EPCAM, GREM1, MITF, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53
Multigenetic panel
Breast cancer
Spanish
-
-
Breast cancer, Ovarian cancer
1
Jesica Ramirez-Hospital Central de Mendoza
+/+
15
c.3815C>G
r.(?)
p.(Ser1272*)
Hetero
N/A
-
Unknown
g.112839409C>G
-
APC_000026
-
-
DNA
SEQ-NG
27-aug-2018
GENDA, COLOR
Hereditary Cancer Risk Test (30 genes)
Multigenetic panel
-
Russian-Ukrainian
-
-
-
1
Pablo Kalfayan-Hospital Italiano
+?/+?
16
c.3920T>A
r.(?)
p.(Ile1307Lys)
Hetero
no
RISK FACTOR
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG, CNV
29-jul-2019
GENOS, COLOR
Hereditary Cancer Risk Test (30 Genes)
Multigenetic panel
Glioblastoma, Hodgkin lymphoma, Melanoma, Skin cancer
Polish-Ucranian
-
CIA (antec ambos/NO explica cuadro)
Glioblastoma Multiform, Melanoma
1
Lina Nuñez-Hospital Alemán
+?/+?
16
c.3920T>A
r.(?)
p.(Ile1307Lys)
Homo
no
RISK FACTOR
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG, CNV
24-jul-2019
GENOS, COLOR
Hereditary Cancer Risk Test (30 genes)
Multigenetic panel
Breast cancer
Lithuanian-Russian-Jew
-
(antec ambos/NO explica cuadro)
Breast cancer, Melanoma
1
Lina Nuñez-Private Practice
+?/+?
16
c.3920T>A
r.(3920u>a)
p.(Ile1307Lys)
Hetero
no
RISK FACTOR
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG
21-apr-2021
Invitae
Panel Invitae Multi-Cancer (84 genes)
Multigenetic panel
--
Italian/Italian
-
-
-
1
Cecilia Montes-IMGO
+?/+?
16
c.3920T>A
r.(3920u>a)
p.(Ile1307Lys)
Hetero
BRCA2
RISK FACTOR
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG
13-nov-2020
Genos/Color
Panel GENOS (30 genes) APC, ATM, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EPCAM, FLCN, GREM1, MLH1, MSH2, MSH6, MUTYH, NBN, NTHL1, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53
Multigenetic panel
Breast cancer
Italian
-
-
Breast cancer
1
Lina Nuñez-Hospital Alemán
+?/?
16
c.3920T>A
r.(3920u>a)
p.(Ile1307Lys)
Hetero
no
RISK FACTOR
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG
25-feb-2021
Genda
Panel de (30 genes) APC, ATM, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EPCAM, FLCN, GREM1, MLH1, MSH2, MSH6, MUTYH, NBN, NTHL1, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53
Multigenetic panel
Breast cancer
Amerindian
-
-
Breast cancer
1
Lina Nuñez-Hospital Alemán
+?/+?
16
c.3920T>A
r.(3920u>a)
p.(Ile1307Lys)
Hetero
MSH6
RISK FACTOR
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG
20-jun-2022
Genia/Invitae
Invitae Multi-cancer panel (84 genes)
Multigenetic panel
--
Spanish/Spanish
-
-
-
1
Pablo Kalfayan-Hospital Italiano
+?/?
16
c.3920T>A
r.(3920u>a)
p.(Ile1307Lys)
Hetero
no
RECLASSIFIED JULY 2022. RISK FACTOR
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG
10-jun-2022
Genia/Invitae
Invitae Common Hereditary Cancers Panel (47 genes) APC, ATM, AXIN2, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, CTNNA1, DICER1, EPCAM, GREM1, HOXB13, KIT, MEN1, MLH1, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NTHL1, PALB2, PDGFRA, PMS2, POLD1, POLE, PTEN, RAD50, RAD51C, RAD51D, SDHA, SDHB, SDHC, SDHD, SMAD4, SMARCA4, STK11, TP53, TSC1, TSC2, VHL
Multigenetic panel
--
Russian (ashkenazi)/Russian(ashkenazi)
-
-
-
1
Pablo Kalfayan-Hospital Italiano
+?/?
16
c.3920T>A
r.(3920u>a)
p.(Ile1307Lys)
Hetero
FANCC
RISK FACTOR
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG, CNV
28-nov-2023
CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS
ACD, AIP, AKT1, APC, ATM, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CASR, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, CHEK2, DICER1, EPCAM, FANCA, FANCC, FANCL, FANCM, FH, FLCN, GALNT12, GREM1, HOXB13, KIT, LZTR1, MAX, MEN1, MET, MITF, MLH1, MRE11A, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NF2, NTHL1, PALB2, PIK3CA, PMS2, POLD1, POLE, POT1, PTEN, RAD50, RAD51B, RAD51C, RAD51D, RB1, RET, RINT1, SDHA, SDHAF2, SDHB, SDHC, SDHD, SMAD4, SMARCA4, SMARCB1, SPRED1, STK11, TERF2IP, TERT, TMEM127, TP53, TSC1, TSC2, VHL, XRCC2.
Multigenetic panel
Colon cancer, Colonic oligoliposis
jew Ashkenazi -Sefaradí
-
-
Attenuated familial adenomatous polyposis
1
Guillermo Alberto-Instituto Fleming
+?/?
16
c.3920T>A
r.(3920u>a)
p.(Ile1307Lys)
Hetero
no
RISK FACTOR
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG
23-jan-2024
GENDA, CENTOGENE
Panel ampliado de Cáncer Hereditario (67 genes) APC, ATM, AXIN2, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, DICER1, DIS3L2, EPCAM, FANCC, FH, FLCN, GALNT12, HOXB13, KIT, MC1R, MEN1, MET, MITF, MLH1, MLH3, MRE11, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NTHL1, PALB2, PMS2, POLD1, POLE, POT1, PRSS1, PTCH1, PTEN, RAD50, RAD51C, RAD51D, RECQL, RET, RNF43, SDHA, SDHAF2, SDHB, SDHC, SDHD, SMAD4, SMARCA4, STK11, TP53, TSC1, TSC2, VHL, WT1, XRCC2, XRCC3, RPS20. y APC c.3920T>, A
Multigenetic panel
N/A
jew (Ashkenazi)
-
-
Lynch syndrome
1
Guillermo Alberto-Instituto Fleming
?/?
16
c.3920T>A
r.(3920u>a)
p.(Ile1307Lys)
Hetero
CHEK2
RISK FACTOR
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG
30-mar-2022
GENDA, INVITAE
Invitae Multi-cancer panel (84 genes)
Multigenetic panel
Breast cancer
Spanish / Italian
-
-
Breast cancer
1
Jesica Ramirez-Hospital Central de Mendoza
+?/?
16
c.3920T>A
r.(3920u>a)
p.(Ile1307Lys)
Hetero
no
-
Unknown
g.112839514T>A
-
APC_000032
-
-
DNA
SEQ-NG
16-aug-2022
GENDA, COLOR
Panel (29 genes) ATM, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A (p14ARF), CDKN2A (p16INK4a), CHEK2, EPCAM, GREM1, MITF, MLH1, MSH2, MSH6, MUTYH, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, SMAD4, STK11, TP53.
Multigenetic panel
Breast cancer
Argentinean/Bolivian
-
-
Breast cancer
1
Jesica Ramirez-Hospital Central de Mendoza
./+?
15
c.4183dupA
r.(?)
p.(Ser1395Lysfs*3)
Hetero
no
-
Unknown
g.112839777dupA
-
APC_000052
-
-
DNA
SEQ
05-feb-2019
CIBIC
Sanger APC
Known familial mutation
-
Spanish
-
-
-
1
Marcela Lopez-CEMAFE
./+?
15
c.4183dupA
r.(?)
p.(Ser1395Lysfs*3)
Hetero
no
-
Unknown
g.112839777dupA
-
APC_000052
-
-
DNA
SEQ
05-feb-2019
CIBIC
Sanger APC
Known familial mutation
-
Spanish
-
-
-
1
Marcela Lopez-CEMAFE
+/+?
15
c.4183dupA
r.(?)
p.(Ser1395Lysfs*3)
Hetero
no
-
Unknown
g.112839777dupA
-
APC_000052
-
-
DNA
SEQ-NG
01-oct-2018
CIBIC/Héritas
Panel Polipomatosis adenomatosa familiar (5 genes) APC, BMPRA1, MUTYH, PTEN, SMAD4
Multigenetic panel
-
Spanish
-
-
-
1
Marcela Lopez-CEMAFE
./+?
15
c.4183dupA
r.(?)
p.(Ser1395Lysfs*3)
Hetero
no
-
Unknown
g.112839777dupA
-
APC_000052
-
-
DNA
SEQ
24-oct-2020
CIBIC
Sanger APC
Known familial mutation
-
Spanish
-
-
-
1
Marcela Lopez-CEMAFE
?/?
15
c.4196G>A
r.(?)
p.(Arg1399His)
Hetero
no
-
Unknown
g.112839790G>A
-
APC_000042
-
-
DNA
CNV, SEQ-NG
20-mar-2020
Fares Taie
Panel 30 genes (APC, ATM, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, EPCAM, FLCN, GREM1, MLH1, MSH2, MSH6, MUTYH, NBN, MTHL1, PA
Multigenetic panel
Breast cancer
Italian-Spanish-French
-
-
Pancreatic cancer, Prostate cancer
1
Silvina Sisterna-Hospital de Comunidad
-?/-
15
c.4326T>A
r.(=)
p.(=)
Hetero
no
RECLASSIFIED JUNE 2019
Unknown
g.112839920T>A
-
APC_000023
-
-
DNA
SEQ-NG, z-score-CNV
12-dic-2017
Héritas
Panel Héritas (24 genes) BRCA1-BRCA2-PTEN-TP53-ATM-CDH1-CHEK2-NBN-NF1-PALB2-STK11-BRIP1-RAD51C-RAD51D-MLH1-MSH2-MSH6-PMS2-APC-MUTYH-BMPR1A-SMAD4-CDKN2A-CDK4
Multigenetic panel
-
Caucasian
-
-
-
1
Gonzalo Tabares-CEMA
-/-
15
c.4326T>A
r.(=)
p.(=)
Hetero
APC
-
Unknown
g.112839920T>A
-
APC_000023
-
-
DNA
SEQ-NG
5-dec-2018
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
-
Italian
-
CIA (antec personales/explica cuadro)
-
1
Maria Laura Gonzalez-Hospital Italiano
-?/-
15
c.4360A>G
r.(?)
p.(Lys1454Glu)
Hetero
no
RECLASSIFIED JULY 2022
Unknown
g.112839954A>G
-
APC_000029
-
-
DNA
SEQ-NG
16-may-2018
Héritas
Panel Héritas (25 genes) APC,ATM,BMPR1A,BRCA1,BRCA2,BRIP1,CDH1,CDK4,CDKN2A,CHEK2,MLH1,MSH2,MSH6,MUTYH,NBN,NF1,PALB2,PTEN,RAD51C,RAD51D,SMAD4,STK11,TP53,EPCAM
Multigenetic panel
--
Uruguayan
-
-
-
1
Laura Vargas Roig-IMBECU
?/?
15
c.4361A>T
r.(?)
p.(Lys1454Ile)
Hetero
no
RECLASSIFIED JUNE 2019
Unknown
g.112839955A>T
-
APC_000027
-
-
DNA
SEQ-NG
27-aug-2018
GENDA, COLOR
Hereditary Cancer Risk Test (30 genes)
Multigenetic panel
-
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
?/-?
15
c.4370C>T
r.(?)
p.(Ala1457Val)
Hetero
no
-
Unknown
g.112839964C>T
-
APC_000043
-
-
DNA
SEQ-NG
17-may-2021
Invitae
Panel Invitae Multi-cáncer
Multigenetic panel
-
Italian; Spanish
-
-
-
1
Jesica Ramirez-Hospital Central de Mendoza
?/-?
15
c.4370C>T
r.(?)
p.(Ala1457Val)
Hetero
no
-
Unknown
g.112839964C>T
-
APC_000043
-
-
DNA
SEQ-NG
25-jun-2021
Invitae
Panel Invitae Multi-cáncer
Multigenetic panel
Breast cancer
Spanish
-
-
Breast cancer
1
Jesica Ramirez-Hospital Central de Mendoza
-/-
15
c.4479G>A
r.(=)
p.(=)
Hetero
APC
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG, z-score-CNV
3-may-2017
Héritas
-
-
-
European
-
-
-
1
Alejandra Mampel-Hospital Universitario de Mendoza
-/-
15
c.4479G>A
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
9-feb-2017
Genia
-
-
-
Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
15
c.4479G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
4-jul-2016
CEMIC
-
-
Healthy/Control
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
15
c.4479G>A
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
15-mar-2017
CEMIC
-
-
-
Spanish
-
-
-
1
Alejandra Mampel-COIR
-/-
15
c.4479G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
22-mar-2017
CEMIC
-
-
-
Spanish
-
-
-
1
Pablo Kalfayan-CEMIC
-/-
15
c.4479G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
9-may-2017
CEMIC
-
-
-
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
15
c.4479G>A
r.(=)
p.(=)
Homo
APC
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
6-sep-2017
Genia
-
-
-
Spanish
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
15
c.4479G>A
r.(=)
p.(=)
Homo
APC
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
5-dec-2018
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
-
Italian
-
CIA (antec personales/explica cuadro)
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
15
c.4479G>A
r.(=)
p.(=)
Hetero
MUTYH
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
16-apr-2019
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
-
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
15
c.4479G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
22-mar-2019
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
--
Spanish
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
15
c.4479G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
3-abr-2019
Dasa Genómica - Genia, Hospital Italiano de Buenos Aires
-
Specific pathology
--
Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
15
c.4479G>A
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
CNV, SEQ-NG
28-mar-2018
IACA
Panel (APC, ATM, BMPR1A, BRCA1, BRCA2, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, SMAD4, STK11, TP53)
Multigenetic panel
Breast cancer
Argentinian
-
-
Breast cancer, Colon cancer
1
Silvina Sisterna-Hospital de Comunidad
-/-
15
c.4479G>A
r.(=)
p.(=)
Hetero
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
22-nov-2019
Biogenotec
Panel (APC, ATM, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, MLH1, MSH2, MSH6, MUTYH, NBN, NF1, PALB2, PMS2, PTEN, RAD51D, RAD51D, SMAD4, STK11, TP53, EPCAM)
Multigenetic panel
-
Unknown
-
-
-
1
Laura Vargas Roig-IMBECU
-/-
15
c.4479G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
SEQ-NG
24-aug-2020
CEMIC
-
Specific pathology
--
Spanish-Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
-/-
15
c.4479G>A
r.(=)
p.(=)
Homo
no
-
Unknown
g.112840073G>A
-
APC_000008
-
-
DNA
CNV, SEQ-NG
27-nov-2019
Invitae
(deriv. Genesia) Invitae Multi-Cancer Panel (84 genes)
Multigenetic panel
Colon cancer
Spanish-Italian
-
-
Colon cancer
1
Lina Nuñez-Private Practice
+/+
16
c.4508C>A
r.(4508c>a)
p.(Ser1503*)
Hetero
N/A
-
Unknown
g.112840102C>A
-
APC_000057
-
-
DNA
SEQ-NG
01-apr-2022
PRICAI-Primer Centro Argentino de Inmunogenética-Fundación Favaloro
Panel NGS para Poliposis Adenomatosa Familiar (mutaciones puntuales) (10 genes) APC, AXIN2, BMPR1A, GREM1, MSH, MUTYH, PTEN, POLD1, POLE, SMAD4
Multigenetic panel
--
Italian/Italian
-
-
-
1
Maria Laura Gonzalez-Hospital Italiano
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