Variant #0000003192 (NC_000023.11:g.89100709C>T, WAS(NM_000377.3):c.28C>T)

Individual ID 00000832
Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.89100709C>T
Published as WAS c.28C>T
Reference Intan Juliana Abd Hamid et al. (2020),dbSNP
DB-ID WAS_000002 See all 2 reported entries
dbSNP ID rs202182978
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Noorzalifah Binti Mazuki
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Noorzalifah Binti Mazuki
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
WAS NM_000377.3 ?/. - c.28C>T WAS c.28C>T r.(?) p.(Pro10Ser) ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000944 DNA ? WAS 3 Noorzalifah Binti Mazuki