Variant #0000980981 (NC_000014.8:g.68963847G>A, NC_000014.8(NM_133509.3):c.1036+28880G>A (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.68963847G>A
DNA change (hg38) -
Published as RAD51B(NM_002877.6):c.1043G>A (p.(Gly348Glu))
ISCN -
DB-ID RAD51B_000024
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD51B NM_002877.5 ?/. - c.1043G>A r.(?) p.(Gly348Glu)
RAD51B NM_133509.3 ?/. - c.1036+28880G>A r.(=) p.(=)


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