Variant #0000552926 (NC_000014.8:g.68331718_68331720del, NC_000014.8(NM_133509.3):c.316-2_316del (RAD51B))

Chromosome 14
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.68331718_68331720del
DNA change (hg38) g.67865001_67865003del
Published as RAD51B(NM_001321809.1):c.316-2_316del (p.?)
ISCN -
DB-ID RAD51B_000008
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD51B NM_002877.5 ?/. - c.316-2_316del r.spl? p.?
RAD51B NM_133509.3 ?/. - c.316-2_316del r.spl? p.?


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