Variant #0000002366 (NC_000013.11:g.32337464C>T, NM_000059.3:c.3109C>T (BRCA2))

Individual ID 00000512
Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32337464C>T
Published as -
Reference Timothy R Rebbeck et al.(2018)
DB-ID BRCA2_000054 See all 6 reported entries
dbSNP ID rs80358557
Frequency 3/64 families
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-03-15 10:24:36 +08:00 (CST)
Date last edited 2021-08-01 12:31:35 +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.3109C>T - r.(?) p.(Gln1037*) - Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000564 DNA SEQ BRCA2 45 Nur Aisyah Athirah