Variant #0000009201 (NC_000017.11:g.35107055T>C, RAD51D(NM_002878.3):c.413A>G)

Individual ID 00001783
Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.35107055T>C
Reference -
DB-ID RAD51D_000011
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Jose Llugdar-IMOC
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)     

Protein     

Zygosity     

Co_ocurrence     

RNA change     

Review status     
RAD51D NM_002878.3 -?/-? 5 c.413A>G p.(Asn138Ser) Hetero no r.(?) -



Screenings


AscendingScreening ID     

Template     

Technique     

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Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000002063 DNA SEQ-NG CEMIC Panel (11 genes) ATM, BRCA1, BRCA2, BARD1, CHEK2, MSH6, NBN, PALB2,PTEN, RAD51C, RAD51D. 22-jul-2021 Multigenetic panel ATM, BARD1, BRCA1, BRCA2, CHEK2, MSH6, NBN, PALB2, PTEN, RAD51C, RAD51D 1 Jose Llugdar-IMOC