Variant #0000006755 (NC_000013.11:g.32338162T>C, BRCA2(NM_000059.3):c.3807T>C)

Individual ID 00001134
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.32338162T>C
Reference -
DB-ID BRCA2_000001 See all 179 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jose Llugdar-Clínica Reina Fabiola
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 -/- 11 c.3807T>C r.(=) p.(=) Hetero no -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000001359 DNA SEQ-NG Clinica Universitaria Reina Fabiola - 24-abr-2019 Specific pathology BRCA1, BRCA2 16 Jose Llugdar-Clínica Reina Fabiola