Variant #0000576313 (NC_000023.10:g.48933311_48933312dup, NM_007075.3:c.620_621dup (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.48933311_48933312dup
DNA change (hg38) g.49075652_49075653dup
Published as WDR45(NM_007075.3):c.620_621dupTA (p.V208*)
ISCN -
DB-ID WDR45_000035
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-19 21:40:28 +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.620_621dup r.(?) p.(Val208Ter)
PRAF2 NM_007213.1 +/. - c.-1666_-1665dup r.(?) p.(=)


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