Variant #0000334052 (NC_000023.10:g.48931481G>A, NM_007075.3:c.*981C>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.48931481G>A
DNA change (hg38) g.49073822G>A
Published as PRAF2(NM_007213.1):c.166C>T (p.(Leu56Phe))
ISCN -
DB-ID PRAF2_000001
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) 0.00378 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR45 NM_007075.3 -?/. - c.*981C>T r.(=) p.(=)
PRAF2 NM_007213.1 -?/. - c.166C>T r.(?) p.(Leu56Phe)


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