Variant #0000810463 (NC_000023.10:g.48935414G>T, NC_000023.10(NM_007075.3):c.131-8C>A (WDR45))

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.48935414G>T
DNA change (hg38) -
Published as WDR45(NM_007075.3):c.131-8C>A
ISCN -
DB-ID WDR45_000140
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) 6.0E-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 2021-09-17 14:40:49 +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.131-8C>A r.(=) p.(=)
PRAF2 NM_007213.1 ?/. - c.-3768C>A r.(?) p.(=)


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