Variant #0000319872 (NC_000019.9:g.36549690C>T, NM_001083961.1:c.186C>T (WDR62))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36549690C>T
DNA change (hg38) g.36058788C>T
Published as WDR62(NM_001083961.1):c.186C>T (p.L62=)
ISCN -
DB-ID WDR62_000009 See all 2 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) 0.17892 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-15 17:40:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR62 NM_001083961.1 -/. - c.186C>T r.(?) p.(Leu62=)
THAP8 NM_152658.2 -/. - c.-4571G>A r.(?) p.(=)


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