Variant #0000893174 (NC_000016.9:g.732216C>T, NM_005861.2:c.721C>T (STUB1))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.732216C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID JMJD8_000025
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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JMJD8 NM_001005920.2 ?/. - c.*578G>A r.(=) p.(=)
STUB1 NM_005861.2 ?/. - c.721C>T r.(?) p.(Arg241Trp)
WDR24 NM_032259.2 ?/. - c.*2518G>A r.(=) p.(=)


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