Variant #0001045338 (NC_000013.10:g.32937506G>C, NM_000059.3:c.8167G>C (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.32937506G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID BRCA2_000290 See all 63 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs41293511
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-06-11 17:09:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +/. - c.8167G>C r.(?) p.(Asp2723His) -


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