Variant #0000053582 (NC_000013.10:g.32930730C>T, NM_000059.3:c.7601C>T (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.32930730C>T
DNA change (hg38) g.32356593C>T
Published as A2534V
ISCN -
DB-ID BRCA2_000214 See all 10 reported entries
Variant remarks Protein likelihood ratio model; inconclusive
Reference PubMed: Karchin 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 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 17:15:54 +02:00 (CEST)
Date last edited 2020-07-03 15:53:47 +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.7601C>T r.(?) p.Ala2534Val -


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