Variant #0000621869 (NC_000007.13:g.158672426G>C, NM_018051.4:c.625G>C (WDR60))

Chromosome 7
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.158672426G>C
DNA change (hg38) g.158879735G>C
Published as WDR60(NM_001350914.1):c.487G>C (p.E163Q), WDR60(NM_018051.4):c.625G>C (p.(Glu209Gln)), WDR60(NM_018051.5):c.625G>C (p.E209Q)
ISCN -
DB-ID WDR60_000008 See all 3 reported entries
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) 0.00015 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 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR60 NM_018051.4 ?/. - c.625G>C r.(?) p.(Glu209Gln)


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