Variant #0000552928 (NC_000014.8:g.68352648T>G, NM_133509.3:c.515T>G (RAD51B))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.68352648T>G
DNA change (hg38) g.67885931T>G
Published as RAD51B(NM_001321809.1):c.515T>G (p.(Leu172Trp))
ISCN -
DB-ID RAD51B_000010
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) 0.01322 View details
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 2023-04-16 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.515T>G r.(?) p.(Leu172Trp)
RAD51B NM_133509.3 -?/. - c.515T>G r.(?) p.(Leu172Trp)


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