Variant #0000926344 (NC_000016.9:g.732049T>C, NM_005861.2:c.642T>C (STUB1))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.732049T>C
DNA change (hg38) -
Published as STUB1(NM_001293197.1):c.426T>C (p.L142=), STUB1(NM_005861.4):c.642T>C (p.L214=)
ISCN -
DB-ID JMJD8_000012 See all 2 reported entries
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) 0.00375 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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.*745A>G r.(=) p.(=)
STUB1 NM_005861.2 -/. - c.642T>C r.(?) p.(Leu214=)
WDR24 NM_032259.2 -/. - c.*2685A>G r.(=) p.(=)


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