Variant #0000982072 (NC_000016.9:g.732400C>G, NM_005861.2:c.823C>G (STUB1))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.732400C>G
DNA change (hg38) -
Published as STUB1(NM_005861.4):c.823C>G (p.(Leu275Val))
ISCN -
DB-ID JMJD8_000033
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.*394G>C r.(=) p.(=)
STUB1 NM_005861.2 +/. - c.823C>G r.(?) p.(Leu275Val)
WDR24 NM_032259.2 +/. - c.*2334G>C r.(=) p.(=)


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