Variant #0000727294 (NC_000019.9:g.36546014dup, NM_001083961.1:c.141dup (WDR62))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.36546014dup
DNA change (hg38) -
Published as WDR62(NM_001083961.2):c.141dupA (p.L48Tfs*32)
ISCN -
DB-ID WDR62_000078
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
WDR62 NM_001083961.1 +?/. - c.141dup r.(?) p.(Leu48ThrfsTer32)
CLIP3 NM_015526.2 +?/. - c.-22447dup r.(?) p.(=)
THAP8 NM_152658.2 +?/. - c.-895dup r.(?) p.(=)


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