Variant #0000054116 (NC_000013.10:g.32936732G>C, NM_000059.3:c.7878G>C (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32936732G>C
DNA change (hg38) g.32362595G>C
Published as W2626C
ISCN -
DB-ID BRCA2_000238 See all 18 reported entries
Variant remarks Embryonic stem cell assay DSS1 interaction not affected; reduced complementation, HR deficient
Reference PubMed: Biswas 2011
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Åsa Ehlén
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2012-03-24 16:39:56 +01:00 (CET)
Date last edited 2020-07-03 15:58:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +?/. 17 c.7878G>C r.(?) p.Trp2626Lys -


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