Variant #0000315396 (NC_000023.10:g.48933578C>A, NM_007075.3:c.466G>T (WDR45))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.48933578C>A
DNA change (hg38) g.49075919C>A
Published as WDR45(NM_007075.3):c.466G>T (p.E156*)
ISCN -
DB-ID WDR45_000014
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-19 21:40:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR45 NM_007075.3 +/. - c.466G>T r.(?) p.(Glu156Ter)
PRAF2 NM_007213.1 +/. - c.-1932G>T r.(?) p.(=)


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