Variant #0000313065 (NC_000019.9:g.36546015C>T, NM_001083961.1:c.142C>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.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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




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.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.