Variant #0000255790 (NC_000023.10:g.48549510A>G, NM_000377.2:c.1466A>G (WAS))

Chromosome X
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.48549510A>G
DNA change (hg38) g.48691119A>G
Published as WAS(NM_000377.2):c.1466A>G (p.D489G, p.(Asp489Gly))
ISCN -
DB-ID WAS_000035 See all 2 reported entries
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WAS NM_000377.2 ?/. - c.1466A>G r.(?) p.(Asp489Gly)
SUV39H1 NM_003173.2 ?/. - c.-5666A>G r.(?) p.(=)


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