Variant #0000002522 (NC_000013.11:g.32379431C>T, BRCA2(NM_000059.3):c.8869C>T)

Individual ID 00000543
Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.32379431C>T
Published as -
Reference Ava Kwong et al.(2016)
DB-ID BRCA2_000011 See all 4 reported entries
dbSNP ID rs276174913
Frequency -
Variant remarks Mutation type: Nonsense
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
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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 +/. 22 c.8869C>T - r.(?) p.(Gln2957*) - Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000595 DNA SEQ BRCA2 4 Nur Aisyah Athirah