Variant #0000000049 (NC_000013.11:g.32327154T>C, NC_000013.11(NM_000059.3):c.631+541T>C (BRCA2))

Individual ID 00000002
Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32327154T>C
Published as -
Reference E Thirthagiri et al.(2008)dbSNPClinVar
DB-ID BRCA2_000044
dbSNP ID rs115974024
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Date created 2017-11-21 02:35:54 +08:00 (CST)
Date last edited 2021-08-22 10:17:18 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
BRCA2 NM_000059.3 -/. - c.631+541T>C - r.(=) p.(=) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000002 DNA ? BRCA2 1 MyHVP