Variant #0000865382 (NC_000017.10:g.56770066C>T, NM_058216.1:c.62C>T (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.56770066C>T
DNA change (hg38) -
Published as RAD51C(NM_002876.2):c.62C>T (p.(Pro21Leu))
ISCN -
DB-ID TEX14_000024
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
TEX14 NM_001201457.1 ?/. - c.-768G>A r.(?) p.(=) -
RAD51C NM_058216.1 ?/. - c.62C>T r.(?) p.(Pro21Leu) -


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