Variant #0001042185 (NC_000017.10:g.73987676C>A, NM_004035.6:c.-12522G>T (ACOX1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73987676C>A
DNA change (hg38) -
Published as TEN1(NM_001113324.3):c.222C>A (p.(Ile74=))
ISCN -
DB-ID CDK3_000003
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) 0.00088 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 2025-05-05 21:14:00 +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     
TEN1 NM_001113324.2 -?/. - c.222C>A r.(?) p.(=)
CDK3 NM_001258.2 -?/. - c.-9387C>A r.(?) p.(=)
ACOX1 NM_004035.6 -?/. - c.-12522G>T r.(?) p.(=)
TEN1-CDK3 NR_037709.1 -?/. - n.523C>A r.(?) -


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