Variant #0000002762 (NC_000013.11:g.32362509T>C, NC_000013.11(NM_000059.3):c.7806-14T>C (BRCA2))

Individual ID 00000329
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.32362509T>C
Reference -
DB-ID BRCA2_000004 See all 280 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florencia Petracchi-CEMIC
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
Date created 2017-12-15 17:20:08 -02:00 (-02)
Date last edited N/A
Options




Variant on transcripts


Gene     
AscendingTranscript     
Affects function     
Exon     
DNA change (cDNA)     
RNA change     
Protein     
Zygosity     
Co_ocurrence     
Review status     
BRCA2 NM_000059.3 -/- 16i c.7806-14T>C r.(=) p.(=) Homo BRCA1 -



Screenings


AscendingScreening ID     
Template     
Technique     
Lab     
Remarks     
Date of test     
Type of test     
Genes screened     
Variants found     
Owner     
0000000377 DNA SEQ-NG CEMIC - 19-jun-2017 - BRCA1, BRCA2 20 Florencia Petracchi-CEMIC

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