Variant #0000004725 (NC_000013.11:g.32398875A>C, BRCA2(NM_000059.3):c.*105A>C)

Individual ID 00000598
Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.32398875A>C
Reference -
DB-ID BRCA2_000059 See all 10 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Lina Nuñez-Private Practice
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Review status     
BRCA2 NM_000059.3 -/- 3'UTR c.*105A>C r.(=) p.(=) Hetero BRCA1 -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000000688 DNA SEQ-NG High Medic Group - 11-nov-2016 Specific pathology panel BRCA1, BRCA2 13 Lina Nuñez-Private Practice