Variant #0001006801 (NC_000023.10:g.48930134C>G, NM_007075.3:c.*2328G>C (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.48930134C>G
DNA change (hg38) -
Published as PRAF2(NM_007213.1):c.355G>C (p.(Gly119Arg))
ISCN -
DB-ID WDR45_000148
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
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.*2328G>C r.(=) p.(=)
PRAF2 NM_007213.1 ?/. - c.355G>C r.(?) p.(Gly119Arg)


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