Variant #0000624634 (NC_000023.10:g.48457218G>A, NM_001166426.1:c.-122G>A (WDR13))

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.48457218G>A
DNA change (hg38) g.48598830G>A
Published as WDR13(NM_001347217.2):c.155G>A (p.R52Q)
ISCN -
DB-ID WDR13_000039
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +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     
WDR13 NM_001166426.1 ?/. - c.-122G>A r.(?) p.(=)
WDR13 NM_017883.4 ?/. - c.155G>A r.(?) p.(Arg52Gln)


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