Variant #0000726539 (NC_000017.10:g.56770084T>C, NM_058216.1:c.80T>C (RAD51C))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.56770084T>C
DNA change (hg38) -
Published as RAD51C(NM_058216.3):c.80T>C (p.L27P)
ISCN -
DB-ID TEX14_000019 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
TEX14 NM_001201457.1 ?/. - c.-786A>G r.(?) p.(=) -
RAD51C NM_058216.1 ?/. - c.80T>C r.(?) p.(Leu27Pro) -


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