Variant #0001006805 (NC_000023.10:g.48932930C>T, NM_007075.3:c.841G>A (WDR45))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48932930C>T
DNA change (hg38) -
Published as WDR45(NM_001029896.1):c.838G>A (p.(Val280Met)), WDR45(NM_007075.3):c.841G>A (p.V281M), WDR45(NM_007075.4):c.841G>A (p.V281M)
ISCN -
DB-ID WDR45_000010 See all 4 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) 0.00668 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR45 NM_007075.3 -/. - c.841G>A r.(?) p.(Val281Met)
PRAF2 NM_007213.1 -/. - c.-1284G>A r.(?) p.(=)


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