chr13:32362582:A>G Detail (hg38) (BRCA2)

Information

Genome

Assembly Position
hg19 chr13:32,936,719-32,936,719 View the variant detail on this assembly version.
hg38 chr13:32,362,582-32,362,582

HGVS

Type Transcript Protein
RefSeq NM_000059.3:c.7865A>G NP_000050.2:p.Asn2622Ser
Ensemble ENST00000380152.8:c.7865A>G ENST00000380152.8:p.Asn2622Ser
ENST00000530893.7:c.7496A>G ENST00000530893.7:p.Asn2499Ser
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:[No Data.]
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:<0.001

Prediction

ClinVar

Clinical Significance Uncertain significance
Review star
Show details
Links
Type Database ID Link
Gene MIM 600185 OMIM
HGNC 1101 HGNC
Ensembl ENSG00000139618 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv382889391 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Uncertain significance 2018-02-16 criteria provided, multiple submitters, no conflicts Breast-ovarian cancer, familial, susceptibility to, 2 germline unknown Detail
Uncertain significance 2022-02-14 criteria provided, multiple submitters, no conflicts Hereditary cancer-predisposing syndrome germline Detail
Uncertain significance 2023-12-22 criteria provided, single submitter hereditary breast ovarian cancer syndrome germline Detail
Uncertain significance 2023-05-25 criteria provided, multiple submitters, no conflicts not provided germline unknown Detail
Uncertain significance 2024-03-07 criteria provided, multiple submitters, no conflicts not specified germline Detail
Uncertain significance 2022-03-27 criteria provided, single submitter Pancreatic cancer, susceptibility to, 2,Familial cancer of breast,Glioma susceptibility 3,Wilms tumor 1,Breast-ovarian cancer, familial, susceptibility to, 2,Malignant tumor of prostate,Fanconi anemia complementation group D1,medulloblastoma unknown Detail
Uncertain significance 2022-03-27 criteria provided, single submitter Pancreatic cancer, susceptibility to, 2,Familial cancer of breast,Glioma susceptibility 3,Wilms tumor 1,Breast-ovarian cancer, familial, susceptibility to, 2,Malignant tumor of prostate,Fanconi anemia complementation group D1,medulloblastoma unknown Detail
Uncertain significance 2022-03-27 criteria provided, single submitter Pancreatic cancer, susceptibility to, 2,Familial cancer of breast,Glioma susceptibility 3,Wilms tumor 1,Breast-ovarian cancer, familial, susceptibility to, 2,Malignant tumor of prostate,Fanconi anemia complementation group D1,medulloblastoma unknown Detail
Uncertain significance 2022-03-27 criteria provided, single submitter Pancreatic cancer, susceptibility to, 2,Familial cancer of breast,Glioma susceptibility 3,Wilms tumor 1,Breast-ovarian cancer, familial, susceptibility to, 2,Malignant tumor of prostate,Fanconi anemia complementation group D1,medulloblastoma unknown Detail
Uncertain significance 2022-03-27 criteria provided, single submitter Pancreatic cancer, susceptibility to, 2,Familial cancer of breast,Glioma susceptibility 3,Wilms tumor 1,Breast-ovarian cancer, familial, susceptibility to, 2,Malignant tumor of prostate,Fanconi anemia complementation group D1,medulloblastoma unknown Detail
Uncertain significance 2022-03-27 criteria provided, single submitter Pancreatic cancer, susceptibility to, 2,Familial cancer of breast,Glioma susceptibility 3,Wilms tumor 1,Breast-ovarian cancer, familial, susceptibility to, 2,Malignant tumor of prostate,Fanconi anemia complementation group D1,medulloblastoma unknown Detail
Uncertain significance 2022-03-27 criteria provided, single submitter Pancreatic cancer, susceptibility to, 2,Familial cancer of breast,Glioma susceptibility 3,Wilms tumor 1,Breast-ovarian cancer, familial, susceptibility to, 2,Malignant tumor of prostate,Fanconi anemia complementation group D1,medulloblastoma unknown Detail
Uncertain significance 2022-03-27 criteria provided, single submitter Pancreatic cancer, susceptibility to, 2,Familial cancer of breast,Glioma susceptibility 3,Wilms tumor 1,Breast-ovarian cancer, familial, susceptibility to, 2,Malignant tumor of prostate,Fanconi anemia complementation group D1,medulloblastoma unknown Detail
Uncertain significance 2023-07-15 criteria provided, single submitter Familial cancer of breast unknown Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.240 Breast-ovarian cancer, familial, susceptibility to, 2 NA CLINVAR Detail
0.174 Breast Cancer, Familial NA CLINVAR Detail
0.391 Hereditary Breast and Ovarian Cancer Syndrome NA CLINVAR Detail
0.128 Neoplastic Syndromes, Hereditary NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND Breast-ovarian cancer, familial, susceptibility to, ... ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND Hereditary cancer-predisposing syndrome ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND Hereditary breast ovarian cancer syndrome ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND not provided ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND not specified ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND multiple conditions ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND multiple conditions ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND multiple conditions ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND multiple conditions ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND multiple conditions ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND multiple conditions ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND multiple conditions ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND multiple conditions ClinVar Detail
NM_000059.4(BRCA2):c.7865A>G (p.Asn2622Ser) AND Familial cancer of breast ClinVar Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs142899125 dbSNP
Genome
hg38
Position
chr13:32,362,582-32,362,582
Variant Type
snv
Reference Allele
A
Alternative Allele
G
East Asian Chromosome Counts (ExAC)
8650
East Asian Allele Counts (ExAC)
0
East Asian Heterozygous Counts (ExAC)
0
East Asian Homozygous Counts (ExAC)
0
East Asian Allele Frequency (ExAC)
0.0
Chromosome Counts in All Race (ExAC)
121330
Allele Counts in All Race (ExAC)
7
Heterozygous Counts in All Race (ExAC)
7
Homozygous Counts in All Race (ExAC)
0
Allele Frequency in All Race (ExAC)
5.76938926893596E-5
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