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 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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TEN1 NM_001113324.2 ?/. - c.*9399C>T r.(=) p.(=)
CDK3 NM_001258.2 ?/. - c.*4238C>T r.(=) p.(=)
EVPL NM_001988.2 ?/. - c.3544G>A r.(?) p.(Val1182Met)
ACOX1 NM_004035.6 ?/. - c.-30588G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.