Variant #0001055295 (NC_000016.9:g.730569C>T, NM_005861.2:c.44C>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.730569C>T
DNA change (hg38) -
Published as STUB1(NM_005861.4):c.44C>T (p.(Ala15Val))
ISCN -
DB-ID JMJD8_000038
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) 8.0E-5 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 2025-11-01 13:22:20 +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.*2225G>A r.(=) p.(=)
STUB1 NM_005861.2 ?/. - c.44C>T r.(?) p.(Ala15Val)
WDR24 NM_032259.2 ?/. - c.*4165G>A r.(=) p.(=)


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