Variant #0000053199 (NC_000013.10:g.32893467G>C, NC_000013.10(NM_000059.3):c.316+5G>C (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32893467G>C
DNA change (hg38) g.32319330G>C
Published as c.316+5G>C
ISCN -
DB-ID BRCA2_000015 See all 3 reported entries
Variant remarks mRNA analysis and splicing reporter minigene; predicted deleterious
Reference PubMed: Bonnet 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Peter Devilee
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Maaike Vreeswijk
Date created 2009-10-03 17:15:53 +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 +/. 3i c.316+5G>C r.spl ? -


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