Variant #0000569775 (NC_000020.10:g.43610466_43610467dup, NC_000020.10(NM_006282.2):c.246-4_246-3dup (STK4))

Chromosome 20
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.43610466_43610467dup
DNA change (hg38) g.44981825_44981826dup
Published as STK4(NM_006282.2):c.246-5_246-4dupTC
ISCN -
DB-ID STK4_000004
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 17:39:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STK4 NM_006282.2 -?/. - c.246-4_246-3dup r.spl? p.?


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