Variant #0000319858 (NC_000023.10:g.48935527G>A, NM_007075.3:c.99C>T (WDR45))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48935527G>A
DNA change (hg38) g.49077868G>A
Published as WDR45(NM_007075.3):c.99C>T (p.N33=)
ISCN -
DB-ID WDR45_000022
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) 7.0E-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 2020-07-19 21:42:44 +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.99C>T r.(?) p.(Asn33=)
PRAF2 NM_007213.1 -?/. - c.-3881C>T r.(?) p.(=)


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