Variant #0000306721 (NC_000014.8:g.68353784G>T, NM_133509.3:c.619G>T (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.68353784G>T
DNA change (hg38) g.67887067G>T
Published as RAD51B(NM_133509.3):c.619G>T (p.V207L)
ISCN -
DB-ID RAD51B_000005 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) 0.00165 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.619G>T r.(?) p.(Val207Leu)
RAD51B NM_133509.3 ?/. - c.619G>T r.(?) p.(Val207Leu)


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