sither
MUTYH (mutY DNA glycosylase)
LOVD v.3.0 Build 29 [
Current LOVD status
]
Log in
Curator:
Instituto Nacional del Cancer
View all genes
View MUTYH gene homepage
View graphs about the MUTYH gene database
Create a new gene entry
View all transcripts
View all transcripts of gene MUTYH
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene MUTYH
View all variants in gene MUTYH
Full data view for gene MUTYH
Create a new data submission
View active genomic custom columns
Enable more genomic custom columns
View all individuals
View all individuals with variants in gene MUTYH
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene MUTYH
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene MUTYH
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
All screenings for gene MUTYH
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.
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
Lab
: Name of the Laboratory that performed the screening.
All options:
3 billion
ARGENETICS
ARGENOMICS - Fundacion Investigar
Bilac - Laboratorio De Alta Complejidad
Biocodices S.A.
Biogenotec
Biogenomic
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
GENERIS
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 Analisis Clinicos Saguir Correa
Laboratorio de Biologia Celular y Molecular IHEM-CONICET CCT Mendoza
Laboratorio de Medicina Genomica - Facultad de Medicina - UNNE
Laboratorio Central
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 Primagen
Laboratorio Tucumán
Laboratorios Turner
Labsis
LACE Laboratorios
LEB (Laboratorio de Especialidades Bioquimicas)
MANLAB
MEDgenomica
PRICAI-Primer Centro Argentino de Inmunogenética-Fundación Favaloro
Sanatorio Allende
Stamboulian Laboratorio
STEM
TRILAB
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
Myriad
Cibic
Turner
Stamboulian
IdenGene
Reference Laboratory Genetics
Macrogen
Hospital de Gastroenterologia " Dr. Carlos Bonorino Udaondo"
IHEM-CONICET CCT Mendoza
Labgenetics (deriv. Pricai)
Invitae (deriv. Genesia)
Genia (deriv. Hospital Italiano)
Invitae (deriv. Genia)
Color (deriv. Genos)
Centogene (deriv. Progenitest)
Gammalab (deriv. Hospital Universitario Austral)
Color (deriv. Genda)
Color (deriv. Genesia)
Invitae (deriv. Genda)
Laboratorio Integral S.R.L.
Trinidad Medical Center
LABORATORIO DRA. CORTELEZZI MARTA
Dasa Genómica
Remarks
: Remarks
Date of test
: Date in which the results of the test were informed to the pacient
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
-
Specific pathology panel
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'
To sort on a certain column, click on the column header or on the arrows. If that column is already selected to sort on, the sort order will be swapped. The column currently sorted on has a darker blue background color than the other columns. The up and down arrows next to the column name indicate the current sorting direction. When sorting on any field other than the default, LOVD will sort secondarily on the default sort column.
75 entries on 1 page. Showing entries 1 - 75.
10 per page
25 per page
50 per page
100 per page
250 per page
500 per page
1000 per page
Legend
How to query
Screening ID
Individual ID
Template
Technique
Lab
Remarks
Date of test
Type of test
Variants found
Owner
0000000058
00000054
DNA
SEQ-NG
Alexander Fleming
-
09-feb-2017
Specific pathology
11
Luisina Bruno-Instituto Fleming
0000000137
00000126
DNA
SEQ-NG;z-score-CNV
Héritas
-
03-may-2017
Specific pathology
10
Alejandra Mampel-Hospital Universitario de Mendoza
0000000144
00000133
DNA
SEQ-NG
CEMIC
-
16-may-2017
Specific pathology
24
Alejandra Mampel-Hospital Universitario de Mendoza
0000000165
00000149
DNA
SEQ-NG
CEMIC
-
18-nov-2015
Specific pathology
23
Pablo Kalfayan-Hospital Italiano
0000000172
00000153
DNA
SEQ-NG
Genia
-
09-feb-2017
Specific pathology
10
Maria Laura Gonzalez-Hospital Italiano
0000000178
00000158
DNA
SEQ-NG
Genia
-
27-mar-2017
Specific pathology
31
Maria Laura Gonzalez-Hospital Italiano
0000000179
00000159
DNA
SEQ-NG
CEMIC
-
04-jul-2016
Specific pathology
9
Maria Laura Gonzalez-Hospital Italiano
0000000181
00000159
DNA
SEQ-NG
CEMIC
-
20-feb-2017
Specific pathology
30
Maria Laura Gonzalez-Hospital Italiano
0000000214
00000188
DNA
SEQ-NG
CEMIC
-
15-mar-2017
Specific pathology
13
Alejandra Mampel-COIR
0000000235
00000208
DNA
SEQ-NG
CEMIC
-
22-mar-2017
Specific pathology
10
Pablo Kalfayan-CEMIC
0000000248
00000153
DNA
MLPA
Genia
-
30-jun-2017
Specific pathology
-
Maria Laura Gonzalez-Hospital Italiano
0000000249
00000153
DNA
SEQ-NG
Genia
-
30-jun-2017
Specific pathology
37
Maria Laura Gonzalez-Hospital Italiano
0000000250
00000218
DNA
SEQ-NG
CEMIC
-
09-may-2017
Specific pathology
11
Maria Laura Gonzalez-Hospital Italiano
0000000251
00000219
DNA
SEQ-NG
CEMIC
-
04-jul-2017
Specific pathology
21
Carlos Vaccaro-Hospital Italiano
0000000258
00000224
DNA
SEQ-NG
CEMIC
-
14-jun-2017
Specific pathology
23
Carlos Vaccaro-Hospital Italiano
0000000333
00000284
DNA
SEQ-NG
Genia
-
06-sep-2017
Specific pathology
10
Maria Laura Gonzalez-Hospital Italiano
0000000334
00000285
DNA
SEQ-NG
Domeq&Lafage
-
30-aug-2017
Specific pathology
26
Carlos Vaccaro-Hospital Italiano
0000000344
00000295
DNA
SEQ-NG
CEMIC
-
11-jul-2017
Specific pathology
24
Pablo Kalfayan-Hospital Italiano
0000000356
00000297
DNA
SEQ-NG
CEMIC
-
11-dec-2015
Specific pathology
21
Carlos Vaccaro-Hospital Italiano
0000000363
00000312
DNA
SEQ-NG
CEMIC
-
11-nov-2016
Specific pathology
39
Lina Nuñez-Private Practice
0000000365
00000313
DNA
SEQ-NG
CEMIC
-
24-feb-2017
Specific pathology
19
Pablo Kalfayan-Hospital Italiano
0000000373
00000325
DNA
SEQ-NG
Genia
-
27-nov-2017
Specific pathology
21
Pablo Kalfayan-Hospital Italiano
0000000525
00000467
DNA
SEQ-NG
CEMIC
-
14-aug-2017
Specific pathology
30
Florencia Petracchi-CEMIC
0000000562
00000498
DNA
SEQ-NG
Clinica Universitaria Reina Fabiola
-
05-mar-2018
Specific pathology
37
Jose Llugdar-Instituto Oulton
0000000577
00000510
DNA
SEQ-NG
CEMIC
-
24-nov-2015
Specific pathology
22
Carlos Vaccaro-Hospital Italiano
0000000585
00000517
DNA
SEQ-NG;z-score-CNV
Héritas
-
20-mar-2018
Specific pathology
-
Erika Stegmayer-Hospital Zenon Santillan
0000000602
00000534
DNA
SEQ-NG
CEMIC
-
19-feb-2018
Specific pathology panel
30
Pablo Kalfayan-Hospital Italiano
0000000626
00000557
DNA
SEQ-NG
Domeq&Lafage
Lynch Panel
02-may-2018
Specific pathology panel
31
Lina Nuñez-Hospital Alemán
0000000696
00000606
DNA
SEQ-NG
CEMIC
-
01-feb-2018
Specific pathology panel
21
Florencia Petracchi-CEMIC
0000000814
00000696
DNA
SEQ-NG
CEMIC
-
26-apr-2018
Specific pathology panel
31
Carlos Vaccaro-Hospital Italiano
0000000912
00000784
DNA
SEQ-NG
CEMIC
-
26-jul-2018
Specific pathology panel
30
Florencia Petracchi-CEMIC
0000000913
00000785
DNA
SEQ-NG
CEMIC
-
02-aug-2018
Specific pathology panel
17
Florencia Petracchi-CEMIC
0000000915
00000787
DNA
SEQ-NG
Domeq&Lafage
-
13-dec-2018
Specific pathology panel
13
Lina Nuñez-Hospital Alemán
0000001028
00000868
DNA
SEQ-NG
Genia
-
16-aug-2018
Specific pathology
24
Pablo Kalfayan-Hospital Italiano
0000001049
00000884
DNA
SEQ-NG
CEMIC
-
25-oct-2018
Specific pathology
11
Pablo Kalfayan-Hospital Italiano
0000001068
00000897
DNA
z-score-CNV
Héritas
-
03-mar-2018
Multigenetic panel
-
Laura Vargas Roig-IMBECU
0000001079
00000901
DNA
z-score-CNV
Héritas
-
16-may-2018
Multigenetic panel
-
Laura Vargas Roig-IMBECU
0000001113
00000924
DNA
SEQ-NG
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
28-feb-2019
Specific pathology
5
Pablo Kalfayan-Hospital Italiano
0000001220
00001018
DNA
SEQ-NG
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
05-dec-2018
Specific pathology
10
Maria Laura Gonzalez-Hospital Italiano
0000001221
00001018
DNA
MLPA
Dasa Genómica - Genia;INVITAE
-
05-dec-2018
Specific pathology
-
Maria Laura Gonzalez-Hospital Italiano
0000001222
00001019
DNA
SEQ-NG
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
16-apr-2019
Specific pathology
9
Maria Laura Gonzalez-Hospital Italiano
0000001223
00001019
DNA
SEQ-NG
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
16-apr-2019
Specific pathology
8
Maria Laura Gonzalez-Hospital Italiano
0000001224
00001019
DNA
MLPA
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
16-apr-2019
Specific pathology
-
Maria Laura Gonzalez-Hospital Italiano
0000001226
00001021
DNA
SEQ-NG
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
30-apr-2019
Specific pathology
15
Carlos Vaccaro-Hospital Italiano
0000001234
00001030
DNA
SEQ
Hospital de Gastroenterologia " Dr. Carlos Bonorino Udaondo"
-
14-jul-2017
Known familial mutation
1
Marina Antelo-Hospital Udaondo
0000001246
00001041
DNA
SEQ-NG
Genia
-
15-jan-2020
Specific pathology
8
Maria Laura Gonzalez-Hospital Italiano
0000001249
00001044
DNA
SEQ-NG
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
06-jun-2019
Specific pathology
12
Carlos Vaccaro-Hospital Italiano
0000001269
00000903
DNA
SEQ
CEMIC
-
08-oct-2019
Germline variant found in somatic testing
1
Lina Nuñez-Private Practice
0000001330
00001115
DNA
SEQ-NG
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
22-mar-2019
Specific pathology
6
Maria Laura Gonzalez-Hospital Italiano
0000001331
00001115
DNA
MLPA
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
22-mar-2019
Specific pathology
-
Maria Laura Gonzalez-Hospital Italiano
0000001332
00001115
DNA
SEQ-NG
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
22-mar-2019
Specific pathology
8
Maria Laura Gonzalez-Hospital Italiano
0000001333
00001116
DNA
SEQ-NG
Genia
-
01-jul-2019
Specific pathology
11
Maria Laura Gonzalez-Hospital Italiano
0000001335
00001017
DNA
MLPA
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
03-apr-2019
Specific pathology
-
Maria Laura Gonzalez-Hospital Italiano
0000001336
00001017
DNA
SEQ-NG
Dasa Genómica - Genia;Hospital Italiano de Buenos Aires
-
03-apr-2019
Specific pathology
7
Maria Laura Gonzalez-Hospital Italiano
0000001339
00001119
DNA
SEQ-NG
CEMIC
-
13-aug-2019
Specific pathology
13
Carlos Vaccaro-Hospital Italiano
0000001408
00001178
DNA
SEQ-NG
CEMIC
-
31-oct-2019
Specific pathology
18
Pablo Kalfayan-Hospital Italiano
0000001491
00001252
DNA
SEQ-NG
Domeq&Lafage
-
27-sep-2019
Multigenetic panel
16
Lina Nuñez-Private Practice
0000001596
00001351
DNA
SEQ-NG
CEMIC
-
09-sep-2019
Multigenetic panel
20
Dolores Mansilla-Instituto Roffo
0000001756
00001488
DNA
SEQ-NG
CEMIC
-
24-aug-2020
Specific pathology
7
Maria Laura Gonzalez-Hospital Italiano
0000001761
00001492
DNA
CNV;SEQ-NG
Héritas
-
31-oct-2019
Multigenetic panel
2
Erika Stegmayer-CIOC
0000001805
00001533
DNA
SEQ-NG
CEMIC
-
03-oct-2019
Multigenetic panel
29
Dolores Mansilla-Instituto Roffo
0000001985
00001709
DNA
SEQ-NG
Genia
NGS Genes Asociados a Síndrome de Linch (6 genes) MLH1, MSH2, MSH6, PMS2, MUTYH y EPCAM
22-dec-2020
Multigenetic panel
1
Pablo Kalfayan-Hospital Italiano
0000001986
00001709
DNA
MLPA
Genia
MLPA Genes Asociados a Síndrome de Linch (6 genes) MLH1, MSH2, MSH6, PMS2, MUTYH y EPCAM
22-dec-2020
Multigenetic panel
-
Pablo Kalfayan-Hospital Italiano
0000002006
00001727
DNA
SEQ-NG
Myriad Genetics
NGS de APC y MUTYH
07-feb-2019
Specific pathology
1
Marcela Lopez - Instituto Donna
0000002016
00001737
DNA
SEQ-NG
CIBIC/Héritas
Panel Polipomatosis adenomatosa familiar (5 genes) APC, BMPRA1, MUTYH, PTEN, SMAD4
01-oct-2018
Multigenetic panel
1
Marcela Lopez-CEMAFE
0000002020
00001741
DNA
SEQ-NG
CIBIC/Héritas
Panel cáncer de colon hereditario Héritas (14 genes) APC,ATM,BMPR1A,CHEK2, EPCAM,MLH1,MSH2,MSH6,MUTYH,PMS2,PTEN,SMAD4,STK11,TP53
26-jun-2019
Multigenetic panel
1
Marcela Lopez-CEMAFE
0000002252
00001965
DNA
SEQ-NG
Genia
Secuenciacion por NGS de genes asociados a Adenopoliposis Colónica Familiar (PAF) APC, MUTYH
17-feb-2022
Specific pathology
1
Pablo Kalfayan-Hospital Italiano
0000002258
00001971
DNA
SEQ-NG
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
01-apr-2022
Multigenetic panel
1
Maria Laura Gonzalez-Hospital Italiano
0000002529
00002236
DNA
SEQ-NG
Domeq&Lafage
complete gene sequencing: MLH1, MSH2, MSH6, PMS2, APC, MUTYH, GREM1, POLE, POLD1, PTEN, NTHL1, STK11
08-10-20
Multigenetic panel
-
Lina Nuñez-Hospital Alemán
0000002702
00002416
DNA
SEQ-NG;CNV
Laboratorio Tucumán
Hereditary cancer panel (7 genes) APC, MUTYH, POLD1, POLE, PTEN, SMAD4, STK11.
28-apr-2022
Multigenetic panel
1
Erika Stegmayer-CIOC
0000002791
00002489
DNA
SEQ-NG
CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS
Hereditary Cancer panel (14 genes) ATM, BRCA1, BRCA2, CHEK2, EPCAM, HOXB13, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, RAD51C, RAD51D.
02-jun-2022
Multigenetic panel
-
Yolanda Isabel Medina - Hospital Juan D. Perón
0000002979
00002669
DNA
SEQ-NG
Centro de Educación Médica e Investigaciones Clínicas (CEMIC)
-
15-feb-2023
Multigenetic panel
1
Maria Laura Gonzalez-Hospital Italiano
0000004110
00003784
DNA
SEQ-NG
CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS
-
17-jan-2023
Multigenetic panel
1
Ivana Romero-Sanatorio Parque
0000010150
00005939
DNA
SEQ-NG;CNV
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, MENT, MET, MITE, 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, TERF2IR, TERT, TMEM127, TP53, TSC1, TSC2, VHL, XRCC2
31-mar-2026
Multigenetic panel
1
Guillermo Alberto-Instituto Fleming
0000010172
00005961
DNA
SEQ-NG;CNV
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, CDKNZ2A, CHEK2, DICER1, EPCAM, FANCA, FANCC, FANCL, FANCM, FH, FLCN, GALNT12, GREM1, HOXB13, KIT, LZTR1, MAX, MENT, MET, MITF, MLH1, MRE11A, MSH2, MSH3, MSHE6, 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, SMARCAA, SMARCB1, SPRED1, STK11, TERF2IR, TERT, TMEM127, TP53, TSC1, TSC2, VHL, XRCC2
31-mar-2026
Multigenetic panel
1
Agostina Tardivo-Instituto Fleming
10 per page
25 per page
50 per page
100 per page
250 per page
500 per page
1000 per page
Legend
How to query
Powered by
LOVD v.3.0
Build 29
LOVD software ©2004-2023
Leiden University Medical Center