Variant #0000325640 (NC_000017.10:g.74005742C>T, NM_004035.6:c.-30588G>A (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.74005742C>T |
DNA change (hg38) |
g.76009661C>T |
Published as |
EVPL(NM_001320747.1):c.3610G>A (p.V1204M), EVPL(NM_001988.2):c.3544G>A (p.(Val1182Met)) |
ISCN |
- |
DB-ID |
EVPL_000006 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) |
0.00017 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
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) |

Variant on transcripts
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