Variant #0000809394 (NC_000021.8:g.40762774A>T, NM_007341.2:c.-61060A>T (SH3BGR))

Chromosome 21
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.40762774A>T
DNA change (hg38) -
Published as WRB(NM_001350296.1):c.151A>T (p.K51*)
ISCN -
DB-ID SH3BGR_000004
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WRB NM_001146218.1 ?/. - c.151A>T r.(?) p.(Lys51*)
SH3BGR NM_007341.2 ?/. - c.-61060A>T r.(?) p.(=)
LCA5L NM_152505.3 ?/. - c.*15034T>A r.(=) p.(=)


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