Variant #0000863628 (NC_000014.8:g.68331693_68331717del, NC_000014.8(NM_133509.3):c.316-27_316-3del (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.68331693_68331717del
DNA change (hg38) -
Published as RAD51B(NM_001321809.1):c.316-27_316-3del (p.?)
ISCN -
DB-ID RAD51B_000018
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 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD51B NM_002877.5 ?/. - c.316-27_316-3del r.spl? p.?
RAD51B NM_133509.3 ?/. - c.316-27_316-3del r.spl? p.?


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