Variant #0000053466 (NC_000013.10:g.32914438del, NM_000059.3:c.5946del (BRCA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32914438del
DNA change (hg38) g.32340301del
Published as 6174delT
ISCN -
DB-ID BRCA2_000149 See all 179 reported entries
Variant remarks Homology-directed repair assay; as variant control
Reference PubMed: Wu 2005
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00027 View details
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 2020-07-03 15:37:02 +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 ?/. 11 c.5946del r.(?) p.Ser1982fs -


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