Variant #0000325636 (NC_000017.10:g.74004600C>A, NM_004035.6:c.-29446G>T (ACOX1))

Chromosome 17
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.74004600C>A
DNA change (hg38) g.76008519C>A
Published as EVPL(NM_001988.2):c.4686G>T (p.(Glu1562Asp))
ISCN -
DB-ID EVPL_000004
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) 0.00057 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 2018-01-15 20:58:59 +01:00 (CET)
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     
TEN1 NM_001113324.2 ?/. - c.*8257C>A r.(=) p.(=)
CDK3 NM_001258.2 ?/. - c.*3096C>A r.(=) p.(=)
EVPL NM_001988.2 ?/. - c.4686G>T r.(?) p.(Glu1562Asp)
ACOX1 NM_004035.6 ?/. - c.-29446G>T r.(?) p.(=)


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