sither
PALB2 (partner and localizer of BRCA2)
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Curator:
Instituto Nacional del Cancer
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All screenings for gene PALB2
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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:
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
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
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101 entries on 2 pages. Showing entries 1 - 100.
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Screening ID
Individual ID
Template
Technique
Lab
Remarks
Date of test
Type of test
Variants found
Owner
0000000109
00000100
DNA
SEQ-NG
Dasa Genómica - Genia;INVITAE
Invitae Breast Cancer Panel
20-apr-2017
Multigenetic panel
20
Lina Nuñez-Private Practice
0000000197
00000173
DNA
SEQ-NG
Sanatorio Allende
Breast Cancer Panel
2-may-2017
-
2
Norma Rossi-Hospital de Córdoba
0000000205
00000180
DNA
SEQ
CEMIC
Known familial mutation
24-may-2017
-
1
Alejandra Mampel-Hospital Universitario de Mendoza
0000000209
00000184
DNA
SEQ-NG;z-score-CNV
Héritas
Panel Héritas (12 genes)
23-may-2017
-
21
Alejandra Mampel-Hospital Universitario de Mendoza
0000000229
00000202
DNA
SEQ-NG;z-score-CNV
Héritas
Panel Héritas (12 genes)
13-oct-2016
-
6
Laura Vargas Roig-IMBECU
0000000259
00000225
DNA
SEQ-NG;z-score-CNV
Héritas
Panel Héritas (9 genes)
12-jan-2017
-
18
Lina Nuñez-Hospital Alemán
0000000284
00000243
DNA
SEQ-NG
Dasa Genómica - Genia;INVITAE
Invitae Breast Cancer Panel
31-jul-2017
Multigenetic panel
1
Norma Rossi-Hospital de Córdoba
0000000424
00000371
DNA
SEQ-NG
IACA
CNVs screening for BRCA1, BRCA2, PALB2
14-sep-2017
-
18
Alejandra Mampel-Hospital Universitario de Mendoza
0000000432
00000379
DNA
SEQ-NG;z-score-CNV
Héritas
Panel Héritas (8 genes)
10-mar-2017
Multigenetic panel
10
Gonzalo Tabares-CEMA
0000000433
00000380
DNA
SEQ-NG
STEM
Panel Cáncer de mama-ovario Hereditario STEM (11 genes)
1-nov-2017
-
1
Gonzalo Tabares-CEMA
0000000449
00000396
DNA
SEQ-NG;z-score-CNV
Héritas
-
21-jul-2017
Multigenetic panel
28
Gonzalo Tabares-CEMA
0000000459
00000406
DNA
SEQ-NG;z-score-CNV
Héritas
-
19-jul-2017
Multigenetic panel
25
Gonzalo Tabares-CEMA
0000000460
00000407
DNA
SEQ-NG;z-score-CNV
Héritas
-
22-oct-2017
Multigenetic panel
8
Gonzalo Tabares-CEMA
0000000461
00000408
DNA
SEQ-NG
STEM
-
29-nov-2017
Multigenetic panel
1
Gonzalo Tabares-CEMA
0000000462
00000409
DNA
SEQ-NG;z-score-CNV
Héritas
-
25-jul-2017
Multigenetic panel
16
Gonzalo Tabares-CEMA
0000000463
00000410
DNA
SEQ-NG;z-score-CNV
Héritas
Panel Héritas (10 genes)
10-ago-2017
-
5
Gonzalo Tabares-CEMA
0000000464
00000411
DNA
SEQ-NG;z-score-CNV
Héritas
-
22-aug-2017
Multigenetic panel
-
Gonzalo Tabares-CEMA
0000000468
00000414
DNA
SEQ-NG
STEM
Panel STEM (11 genes)
18-dic-2017
Multigenetic panel
1
Gonzalo Tabares-CEMA
0000000503
00000446
DNA
SEQ-NG
Héritas
Panel Héritas (12 genes)
21-sep-2017
-
4
Laura Vargas Roig-IMBECU
0000000506
00000449
DNA
SEQ-NG
Héritas
Panel Héritas (12 genes)
19-jul-2017
-
13
Laura Vargas Roig-IMBECU
0000000510
00000453
DNA
SEQ-NG
Héritas
Panel Héritas (12 genes)
14-aug-2017
-
5
Laura Vargas Roig-IMBECU
0000000561
00000497
DNA
SEQ-NG
CEMIC
Panel CEMIC
3-jan-2018
-
18
Pablo Kalfayan-Hospital Italiano
0000000681
00000594
DNA
SEQ-NG
IACA
CNVs screening for BRCA1, BRCA2, PALB2, RAD51D, RAD51C, TP53
4-may-2018
Multigenetic panel
1
Lina Nuñez-Private Practice
0000000753
00000651
DNA
SEQ-NG;z-score-CNV
Héritas
-
30-jul-2018
Multigenetic panel
1
Alvaro Yanzi-Instituto San Marcos
0000000817
00000506
DNA
SEQ-NG
CEMIC
-
21-may-2018
Multigenetic panel
13
Lina Nuñez-Private Practice
0000000991
00000838
DNA
SEQ-NG
CEMIC
-
21-mar-2019
Multigenetic panel
18
Lina Nuñez-Private Practice
0000001048
00000883
DNA
SEQ
Hospital Privado Centro Médico de Córdoba
-
21-nov-2018
Known familial mutation
2
Cecilia Montes-IMGO
0000001133
00000939
DNA
CNVs;SEQ-NG
IACA
-
14-mar-2019
Multigenetic panel
13
Silvina Sisterna-Hospital de Comunidad
0000001135
00000941
DNA
SEQ-NG
CEMIC
-
21-mar-2019
Multigenetic panel
11
Dolores Mansilla-Instituto Roffo
0000001141
00000946
DNA
SEQ-NG
CEMIC
-
24-apr-2019
Multigenetic panel
2
Dolores Mansilla-Instituto Roffo
0000001157
00000960
DNA
CNVs;SEQ-NG
Héritas
-
26-jul-2019
Multigenetic panel
1
Claudia Martin-Hospital de Córdoba
0000001229
00001024
DNA
CNV;SEQ-NG
IACA
CNV in genes BRCA1, BRCA2, PALB2, RAD51D, RAD51C, TP53
26-sep-2018
Multigenetic panel
27
Silvina Sisterna-Hospital de Comunidad
0000001254
00001048
DNA
SEQ-NG
CEMIC
-
4-aug-2019
Multigenetic panel
15
Claudia Martin-Hospital de Córdoba
0000001283
00001072
DNA
CNV;SEQ-NG
IACA
-
4-oct-2019
Multigenetic panel
24
Silvina Sisterna-Hospital de Comunidad
0000001284
00001073
DNA
CNV;SEQ-NG
IACA
-
27-dec-2019
Multigenetic panel
20
Silvina Sisterna-Hospital de Comunidad
0000001393
00001166
DNA
CNV;SEQ-NG
Invitae (deriv. Genia)
-
24-oct-2019
Multigenetic panel
1
Pablo Kalfayan-Hospital Italiano
0000001407
00001177
DNA
CNV;SEQ-NG
Hospital Universitario Austral
Test realizado en Laboratorio de Derivación
28-jan-2020
Multigenetic panel
1
Pablo Kalfayan-Hospital Italiano
0000001497
00001258
DNA
CNV;SEQ-NG
IACA
-
9-dec-2019
Multigenetic panel
15
Silvina Sisterna-Hospital de Comunidad
0000001514
00001275
DNA
CNV;SEQ-NG
IACA
-
15-apr-2019
Multigenetic panel
18
Silvina Sisterna-Hospital de Comunidad
0000001516
00001277
DNA
CNV;SEQ-NG
IACA
-
29-jul-2019
Multigenetic panel
31
Silvina Sisterna-Hospital de Comunidad
0000001517
00001278
DNA
SEQ-NG
IACA
CNV analysis of BRCA1, BRCA2, PALB2, RAD51D, RAD51C and TP53
26-sep-2018
Multigenetic panel
24
Silvina Sisterna-Hospital de Comunidad
0000001524
00001285
DNA
CNV;SEQ-NG
IACA
CNV test of BRCA1, BRCA2, PALB2, RAD51C, RAD51D, TP53.
2-aug-2018
Multigenetic panel
32
Silvina Sisterna-Hospital de Comunidad
0000001530
00001291
DNA
CNV;SEQ-NG
IACA
-
18-jun-2019
Multigenetic panel
20
Silvina Sisterna-Hospital de Comunidad
0000001533
00001294
DNA
CNV;SEQ-NG
IACA
CNV test of BRCA1, BRCA2, PALB2, RAD51D, RAD51C, TP53
26-sep-2018
Multigenetic panel
23
Silvina Sisterna-Hospital de Comunidad
0000001534
00001295
DNA
CNV;SEQ-NG
IACA
-
24-sep-2019
Multigenetic panel
25
Silvina Sisterna-Hospital de Comunidad
0000001540
00001301
DNA
CNV;SEQ-NG
IACA
-
18-jun-219
Multigenetic panel
12
Silvina Sisterna-Hospital de Comunidad
0000001542
00001303
DNA
CNV;SEQ-NG
IACA
-
21-oct-2019
Multigenetic panel
21
Silvina Sisterna-Hospital de Comunidad
0000001543
00001304
DNA
CNV;SEQ-NG
IACA
-
7-may-2019
Multigenetic panel
22
Silvina Sisterna-Hospital de Comunidad
0000001584
00001343
DNA
CNV;SEQ-NG
Invitae (deriv. Genesia)
-
19-dec-2019
Multigenetic panel
-
Dolores Mansilla-Instituto Roffo
0000001596
00001351
DNA
SEQ-NG
CEMIC
-
9-sep-2019
Multigenetic panel
20
Dolores Mansilla-Instituto Roffo
0000001616
00001367
DNA
SEQ
Hospital Privado Centro Médico de Córdoba
-
17-apr-2020
Known familial mutation
-
Claudia Martin-Hospital de Córdoba
0000001626
00001377
DNA
SEQ
Hospital Privado Centro Médico de Córdoba
-
17-apr-2020
Known familial mutation
1
Claudia Martin-Hospital de Córdoba
0000001627
00001378
DNA
SEQ
Hospital Privado Centro Médico de Córdoba
-
17-apr-2020
Known familial mutation
1
Claudia Martin-Hospital de Córdoba
0000001688
00001434
DNA
CNV;SEQ-NG
Héritas
-
28-sep-2019
Multigenetic panel
2
Erika Stegmayer-CIOC
0000001693
00001439
DNA
CNV;SEQ-NG
Héritas
-
5-jul-2017
Multigenetic panel
16
Laura Vargas Roig-IMBECU
0000001741
00001475
DNA
SEQ-NG
Domeq&Lafage
-
4-may-2020
Multigenetic panel
12
Lina Nuñez-Hospital Alemán
0000001759
00001490
DNA
SEQ-NG
CEMIC
-
25-sep-2019
Multigenetic panel
20
Erika Stegmayer-Inst. Nuestra Señora de las Mercedes
0000001760
00001491
DNA
SEQ-NG
Domeq&Lafage
-
10-oct-2019
Multigenetic panel
19
Erika Stegmayer-CIOC
0000001761
00001492
DNA
CNV;SEQ-NG
Héritas
-
31-oct-2019
Multigenetic panel
2
Erika Stegmayer-CIOC
0000001805
00001533
DNA
SEQ-NG
CEMIC
-
3-oct-2019
Multigenetic panel
29
Dolores Mansilla-Instituto Roffo
0000001816
00001543
DNA
SEQ-NG
Biogenotec
-
14-oct-2020
Multigenetic panel
1
Alejandra Mampel-COIR
0000001835
00001562
DNA
SEQ-NG
Biogenotec
-
13-may-2021
Multigenetic panel
1
Alejandra Mampel-COIR
0000001836
00001563
DNA
SEQ-NG
Biogenotec
-
03-feb-2020
Multigenetic panel
1
Alejandra Mampel-Hospital Universitario de Mendoza
0000001944
00001669
DNA
SEQ-NG
IACA
Panel (13 genes) ATM, BARD1, BRCA1, BRCA2, BRIP1, CHEK2, NBN, PALB2, PTEN,RAD51C, RAD51D, STK11,TP53
27-jan-2021
Multigenetic panel
2
Silvina Sisterna-Hospital de Comunidad
0000001953
00001678
DNA
SEQ
Biogenotec
Sanger Mutación puntual PALB2 y TP53
23-mar-2020
Specific pathology
1
Alejandra Mampel-COIR
0000001954
00001679
DNA
SEQ-NG
Biogenotec
Panel Cáncer de mama y ovario DE 14 GENES (ATM, BRCA1, BRCA2, BRIP1, CHEK2, MLH1, MSH2, MSH6, NBN,PALB2, PMS2, PTEN, STK11, TP53)
29-oct-2020
Multigenetic panel
2
Alejandra Mampel-COIR
0000002011
00001732
DNA
SEQ-NG
CIBIC/Héritas
Sindrome cáncer hereditario mama y ovarios (14 genes) ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53
23-jan-2018
Multigenetic panel
1
Instituto Nacional del Cancer
0000002013
00001734
DNA
SEQ-NG
CIBIC/Héritas
Sindrome cáncer hereditario mama y ovarios (14 genes) ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53
04-oct-2018
Multigenetic panel
1
Marcela Lopez-CEMAFE
0000002021
00001742
DNA
SEQ-NG
CIBIC/Héritas
Sindrome cáncer hereditario mama y ovarios (14 genes) ATM, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53
20-jul-2018
Multigenetic panel
1
Marcela Lopez-CEMAFE
0000002028
00001749
DNA
SEQ-NG
IACA
Panel (13 genes) ATM, BARD1, BRCA1, BRCA2, BRIP1, CHEK2, NBN, PALB2, PTEN,RAD51C, RAD51D, STK11,TP53
01-jan-2020
Multigenetic panel
2
Luisina Bruno-Instituto Fleming
0000002063
00001783
DNA
SEQ-NG
CEMIC
Panel (11 genes) ATM, BRCA1, BRCA2, BARD1, CHEK2, MSH6, NBN, PALB2,PTEN, RAD51C, RAD51D.
22-jul-2021
Multigenetic panel
1
Jose Llugdar-IMOC
0000002087
00001802
DNA
SEQ-NG
Hospital Universitario Austral
Panel (15 genes) ATM, BRCA1, BRCA2, CHEK2, CDH1, EPCAM, MLH1, MSH2, MSH6, NBN, PALB2, PMS2, PTEN, STK11, TP53
02-mar-2021
Multigenetic panel
1
Maria Constanza Vallone-Hospital Austral
0000002117
00001832
DNA
SEQ-NG
Genia/Invitae
Panel cancer mama (12 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, NBN, NF1, PALB2, PTEN, STK11, TP53
01-sep-2021
Multigenetic panel
1
Pablo Kalfayan-Hospital Italiano
0000002161
00001875
DNA
SEQ-NG
IACA
-
15-sep-2021
Multigenetic panel
-
Silvina Sisterna-Hospital de Comunidad
0000002278
00001991
DNA
SEQ
Fundación para el Progreso de la Medicina
Analisis de variante: PALB2(NM_024675.4) c.2964del (p.Val989Ter)
22-jul-2021
Known familial mutation
1
Cecilia Montes-IMGO
0000002353
00002066
DNA
SEQ-NG
Invitae
Invitae Breast Cancer Panel (13 genes) ATM*, BARD1, BRCA1, BRCA2, CDH1, CHEK2, NF1*, PALB2, PTEN*, RAD51C, RAD51D, STK11, TP53
26-may-2022
Multigenetic panel
Not yet submitted
Lina Nuñez-Private Practice
0000002388
00002101
DNA
SEQ-NG
Fares Taie
Panel Cancer mama-ovario (12 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53.
19-aug-2022
Multigenetic panel
-
Silvina Sisterna-Hospital de Comunidad
0000002390
00002103
DNA
SEQ-NG
Fares Taie
Panel Cancer mama-ovario (12 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53.
24-aug-22
Multigenetic panel
2
Silvina Sisterna-Hospital de Comunidad
0000002405
00002118
DNA
SEQ-NG
Fares Taie
Panel Cancer mama-ovario (10 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, RAD51D, TP53.
05-sep-2022
Multigenetic panel
-
Silvina Sisterna-Hospital de Comunidad
0000002412
00002125
DNA
SEQ-NG
Fares Taie
Sindrome cáncer hereditario mama y ovarios (13 genes) ATM, BRCA1, BRCA2, BRIP1, EPCAM, MLH1, MSH2, MSH6, PALB2, PMS2, RAD51C, RAD51D, STK11
28-jul-2021
Multigenetic panel
1
Lina Nuñez-Private Practice
0000002457
00002166
DNA
SEQ-NG
Genesia - Progenitest;Instituto Alexander Fleming;INVITAE
-
01-06-2022
Multigenetic panel
-
Lina Nuñez-Private Practice
0000002461
00002170
DNA
SEQ-NG
Fares Taie
HP-SI-229-CIA
10-11-2022
Multigenetic panel
-
Silvina Sisterna-Hospital de Comunidad
0000002467
00002176
DNA
SEQ
IACA
-
23-09-22
Known familial mutation
1
Silvina Sisterna-Hospital de Comunidad
0000002468
00002177
DNA
SEQ-NG
MEDgenomica
-
22-09-22
Specific pathology
1
Silvina Sisterna-Hospital de Comunidad
0000002498
00002206
DNA
SEQ-NG
Fares Taie
-
12-12-22
Specific pathology
-
Silvina Sisterna-Hospital de Comunidad
0000002512
00002219
DNA
SEQ-NG
Fares Taie
Panel (11 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, RAD51C, RAD51D, TP53
22-12-22
Multigenetic panel
1
Silvina Sisterna-Hospital de Comunidad
0000002516
00002223
DNA
SEQ-NG
Fares Taie
Panel (11 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, PALB2, PTEN, RAD51C, RAD51D, TP53
29-12-22
Multigenetic panel
-
Silvina Sisterna-Hospital de Comunidad
0000002519
00002226
DNA
SEQ-NG
Hospital Privado Centro Médico de Córdoba
PROSTATE CANCER PANEL (12 genes) ATM, BRCA1, BRCA2, CHEK2, EPCAM, MLH1, MSH2, MSH6, NBN, PALB2, PMS2, RAD51D, TP53
28-10-22
Multigenetic panel
-
Claudia Martin-Hospital de Córdoba
0000002549
00000506
DNA
SEQ-NG
CEMIC
complete gene sequencing: BRCA1, BRCA2, TP53, PTEN, STK11, CHEK2, PALB2, ATM, NBN
20-09-18
Multigenetic panel
1
Lina Nuñez-Private Practice
0000002550
00002256
DNA
SEQ-NG
CEMIC
complete gene sequencing: BRCA1, BRCA2, TP53, PTEN, STK11, CHEK2, PALB2, ATM, NBN
04-10-19
Multigenetic panel
-
Lina Nuñez-Private Practice
0000002642
00002382
DNA
SEQ-NG
Laboratorio Fares Taie
Breast and ovarian, BRCA1, BRCA2, PALB2
13-04-23
Specific pathology
-
Silvina Sisterna-Hospital de Comunidad
0000002678
00002303
DNA
SEQ
CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS
NM_024675.4:c.1653T>A (p.Tyr551Ter) , gen PALB2
12-10-22
Known familial mutation
1
Emilia Maldonado-Hospital de Córdoba
0000002693
00002407
DNA
SEQ-NG;arrayCNV
Biocodices S.A.
-
15-06-22
Multigenetic panel
2
Erika Stegmayer-CIOC
0000002697
00002411
DNA
SEQ-NG
CIBIC – Centro de Diagnóstico Médico de Alta Complejidad S.A. - HERITAS
Panel (10 genes) ATM, BRCA1, BRCA2, CDH1, CHEK2, NBN, PALB2, PTEN, STK11, TP53
23-09-21
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.
2-jun-2022
Multigenetic panel
-
Yolanda Isabel Medina - Hospital Juan D. Perón
0000002821
00002520
DNA
SEQ
Fundación para el Progreso de la Medicina
secuenciacion sanger. PALB2 (NM_023675.3): c.1653T>A
16-mar-2023
Known familial mutation
-
Norma Rossi - Sanatorio Allende
0000002897
00002598
DNA
SEQ-NG
Fundación para el Progreso de la Medicina
PALB2, exon 5 c.1965dup (p.(Pro656Serfs*7))
20-04-23
Known familial mutation
1
Norma Rossi - Fundacion Para el Progreso de la Medicina
0000002918
00002618
DNA
SEQ-NG
Fundación para el Progreso de la Medicina
-
27-mar-2023, 29-8-2023
Specific pathology
Not yet submitted
Norma Rossi - Sanatorio Allende
0000003090
00002779
DNA
SEQ
GENDA;Blueprint Genetics
PALB2 c.2514+1G>A
12-jan-2024
Known familial mutation
1
Lina Nuñez-Private Practice
0000003494
00003176
DNA
SEQ
Fundación para el Progreso de la Medicina
PALB2 (NM_024675.3): c.1653T>A
30-oct-2023
Known familial mutation
1
Claudia Martin-Hospital de Córdoba
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