Variant #0000054114 (NC_000013.10:g.32921033G>A, NM_000059.3:c.7007G>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.32921033G>A
DNA change (hg38) g.32346896G>A
Published as R2336H
ISCN -
DB-ID BRCA2_000175 See all 47 reported entries
Variant remarks Embryonic stem cell assay, RNA analysis; aberrant splicing, 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 16:22:41 +01:00 (CET)
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 +?/. 13 c.7007G>A r.spl p.Arg2336His -


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