Variant #0000005359 (NC_000013.11:g.32341276_32341279delTTAA, BRCA2(NM_000059.3):c.6841+80_6841+83delTTAA)

Individual ID 00000707
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.32341276_32341279delTTAA
Reference -
DB-ID BRCA2_000002 See all 146 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Rita Valdez-Hospital Alemán
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Review status     
BRCA2 NM_000059.3 -/- 11i c.6841+80_6841+83delTTAA r.(=) p.(=) Hetero BRCA1 -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000000827 DNA SEQ-NG Domeq&Lafage - 3-oct-2017 Specific pathology panel BRCA1, BRCA2 16 Rita Valdez-Hospital Alemán