Variant #0000054115 (NC_000013.10:g.32930658T>C, NM_000059.3:c.7529T>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.32930658T>C
DNA change (hg38) g.32356521T>C
Published as L2510P
ISCN -
DB-ID BRCA2_000205 See all 6 reported entries
Variant remarks embryonic stem cell assay reduced DSS1 binding; 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) Retrieve
Owner Åsa Ehlén
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2012-03-24 16:35:01 +01:00 (CET)
Date last edited 2020-07-03 15:53:16 +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 +?/. 15 c.7529T>C r.(?) p.Leu2510Pro -


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