Variant #0000863631 (NC_000014.8:g.69061259C>G, NM_133509.3:c.1094C>G (RAD51B))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.69061259C>G
DNA change (hg38) -
Published as RAD51B(NM_133509.3):c.1094C>G (p.(Pro365Arg))
ISCN -
DB-ID RAD51B_000021
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) 0.02951 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 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.*97402C>G r.(=) p.(=)
RAD51B NM_133509.3 -/. - c.1094C>G r.(?) p.(Pro365Arg)


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