Variant #0000624635 (NC_000023.10:g.48458867C>G, NM_001166426.1:c.408C>G (WDR13))

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.48458867C>G
DNA change (hg38) g.48600479C>G
Published as WDR13(NM_001347217.2):c.684C>G (p.S228=)
ISCN -
DB-ID WDR13_000041
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) 1.0E-5 View details
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 2020-07-19 20:59:20 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR13 NM_001166426.1 -?/. - c.408C>G r.(?) p.(Ser136=)
WDR13 NM_017883.4 -?/. - c.684C>G r.(?) p.(Ser228=)


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