Variant #0000002819 (NC_000023.11:g.10196G>T, NM_000377.3:c.1264G>T (WAS))

Individual ID 00000657
Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.10196G>T
Published as -
Reference Mohd Farid Baharin et al.(2016)
DB-ID WAS_000001
dbSNP ID rs1448275854
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-05-27 16:05:09 +08:00 (CST)
Date last edited 2021-09-06 09:49:18 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
WAS NM_000377.3 +/. 10 c.1264G>T - r.(?) p.(Ala422Ser) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000724 DNA SEQ WAS 1 Nur Aisyah Athirah