Variant #0000054096 (NC_000013.10:g.32950929G>A, NC_000013.10(NM_000059.3):c.8754+1G>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.32950929G>A
DNA change (hg38) g.32376792G>A
Published as -
ISCN -
DB-ID BRCA2_000491 See all 8 reported entries
Variant remarks Aberant splicing; predicted deleterious
Reference PubMed: Hansen 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Thomas Hansen
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2011-09-14 14:38:31 +02:00 (CEST)
Date last edited 2019-02-25 21:51:16 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
BRCA2 NM_000059.3 +?/. 21i c.8754+1G>A r.spl ? -


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