Variant #0000692131 (NC_000016.9:g.731512A>C, NM_005861.2:c.433A>C (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.731512A>C
DNA change (hg38) -
Published as STUB1(NM_005861.2):c.433A>C (p.(Lys145Gln)), STUB1(NM_005861.3):c.433A>C (p.K145Q)
ISCN -
DB-ID STUB1_000005 See all 4 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) 0.00063 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JMJD8 NM_001005920.2 ?/. - c.*1282T>G r.(=) p.(=)
STUB1 NM_005861.2 ?/. - c.433A>C r.(?) p.(Lys145Gln)
WDR24 NM_032259.2 ?/. - c.*3222T>G r.(=) p.(=)


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