Variant #0000728981 (NC_000023.10:g.48935407C>G, NC_000023.10(NM_007075.3):c.131-1G>C (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.48935407C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID WDR45_000138
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR45 NM_007075.3 +/. - c.131-1G>C r.spl? p.?
PRAF2 NM_007213.1 +/. - c.-3761G>C r.(?) p.(=)


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