Variant #0000002396 (NC_000013.11:g.32332287C>G, BRCA2(NM_000059.3):c.809C>G)

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.32332287C>G
Published as -
Reference Timothy R Rebbeck et al.(2018)
DB-ID BRCA2_000125 See all 3 reported entries
dbSNP ID rs276174902
Frequency 2/64 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
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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.809C>G - r.(?) p.(Ser270*) - Pathogenic



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000564 DNA SEQ BRCA2 45 Nur Aisyah Athirah