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

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
Date created 2021-08-10 11:51:58 +08:00 (CST)
Date last edited 2022-01-25 09:34:50 +08:00 (CST)
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