chr13:32319330:G>A Detail (hg38) (BRCA2)

Information

Genome

Assembly Position
hg19 chr13:32,893,467-32,893,467 View the variant detail on this assembly version.
hg38 chr13:32,319,330-32,319,330

HGVS

Type Transcript Protein
RefSeq NM_000059.3:c.316+5G>A
Ensemble ENST00000380152.8:c.316+5G>A
ENST00000530893.7:c.-54+5G>A
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Pathogenic
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
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Pathogenic Likely pathogenic 2022-10-17 criteria provided, multiple submitters, no conflicts hereditary breast ovarian cancer syndrome germline unknown Detail
Pathogenic 2018-04-01 reviewed by expert panel Breast-ovarian cancer, familial, susceptibility to, 2 germline Detail
Pathogenic Likely pathogenic 2023-09-25 criteria provided, multiple submitters, no conflicts Hereditary cancer-predisposing syndrome germline Detail
Pathogenic Likely pathogenic 2023-02-21 criteria provided, multiple submitters, no conflicts not provided germline Detail
Pathogenic 2013-04-04 no assertion criteria provided Breast and/or ovarian cancer germline Detail
Pathogenic no assertion criteria provided Malignant tumor of urinary bladder somatic Detail
Pathogenic 2021-08-02 criteria provided, multiple submitters, no conflicts Familial cancer of breast germline 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
0.391 Hereditary Breast and Ovarian Cancer Syndrome NA CLINVAR Detail
Annotation

Annotations

DescrptionSourceLinks
NM_000059.4(BRCA2):c.316+5G>A AND Hereditary breast ovarian cancer syndrome ClinVar Detail
NM_000059.4(BRCA2):c.316+5G>A AND Breast-ovarian cancer, familial, susceptibility to, 2 ClinVar Detail
NM_000059.4(BRCA2):c.316+5G>A AND Hereditary cancer-predisposing syndrome ClinVar Detail
NM_000059.4(BRCA2):c.316+5G>A AND not provided ClinVar Detail
NM_000059.4(BRCA2):c.316+5G>A AND Breast and/or ovarian cancer ClinVar Detail
NM_000059.4(BRCA2):c.316+5G>A AND Malignant tumor of urinary bladder ClinVar Detail
NM_000059.4(BRCA2):c.316+5G>A AND Familial cancer of breast ClinVar Detail
NA DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs81002840 dbSNP
Genome
hg38
Position
chr13:32,319,330-32,319,330
Variant Type
snv
Reference Allele
G
Alternative Allele
A
Genome browser