Variant #0000615059 (NC_000014.8:g.69061228G>A, NM_133509.3:c.1063G>A (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.69061228G>A
DNA change (hg38) g.68594511G>A
Published as RAD51B(NM_133509.3):c.1063G>A (p.A355T)
ISCN -
DB-ID RAD51B_000016
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) 0.00292 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 2019-12-04 15:24:38 +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.*97371G>A r.(=) p.(=)
RAD51B NM_133509.3 -?/. - c.1063G>A r.(?) p.(Ala355Thr)


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