Variant #0000567052 (NC_000019.9:g.36546015C>T, NM_001083961.1:c.142C>T (WDR62))

Chromosome 19
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.36546015C>T
DNA change (hg38) g.36055113C>T
Published as WDR62(NM_001083961.1):c.142C>T (p.L48F, p.(Leu48Phe)), WDR62(NM_001083961.2):c.142C>T (p.L48F)
ISCN -
DB-ID WDR62_000007 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) 0.00723 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.142C>T r.(?) p.(Leu48Phe)
CLIP3 NM_015526.2 -?/. - c.-22448G>A r.(?) p.(=)
THAP8 NM_152658.2 -?/. - c.-896G>A r.(?) p.(=)


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