Variant #0000002882 (NC_000017.11:g.58694954G>A, RAD51C(NM_002876.3):c.169G>A)

Individual ID 00000346
Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.58694954G>A
Reference -
DB-ID RAD51C_000001
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Claudia Martin-Hospital de Córdoba
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)     

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RNA change     

Review status     
RAD51C NM_002876.3 ?/? 2 c.169G>A p.(Ala57Thr) Hetero no r.(?) RECLASSIFIED JUNE 2019



Screenings


AscendingScreening ID     

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Variants found     

Owner     
0000000395 DNA SEQ-NG GENDA;COLOR Hereditary Cancer Risk Test (30 genes) 17-nov-2017 Multigenetic panel - 1 Claudia Martin-Hospital de Córdoba