Variant #0000054119 (NC_000013.10:g.32900700G>A, NM_000059.3:c.581G>A (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.32900700G>A
DNA change (hg38) g.32326563G>A
Published as 809G>A
ISCN -
DB-ID BRCA2_000517 See all 13 reported entries
Variant remarks Mouse ES cell assay, RNA analysis, partial exon 7 deletion ; partial rescue lethality; HR as wt
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) Retrieve
Owner Maaike Vreeswijk
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2012-06-21 11:40:05 +02:00 (CEST)
Date last edited 2019-02-25 21:51:16 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +?/. 7 c.581G>A r.spl p.Thp194* -


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