Variant #0001006808 (NC_000023.10:g.48935335C>T, NM_007075.3:c.202G>A (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.48935335C>T
DNA change (hg38) -
Published as WDR45(NM_001029896.1):c.202G>A (p.(Gly68Ser))
ISCN -
DB-ID WDR45_000152
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.202G>A r.(?) p.(Gly68Ser)
PRAF2 NM_007213.1 -?/. - c.-3689G>A r.(?) p.(=)


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