Variant #0001003675 (NC_000017.10:g.73946976G>A, NM_004035.6:c.1177C>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.73946976G>A
DNA change (hg38) g.75950895G>A
Published as ACOX1(NM_004035.6):c.1177C>T (p.(Arg393Trp))
ISCN -
DB-ID ACOX1_000029
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) 1.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-01-07 15:52:25 +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.-28623G>A r.(?) p.(=)
ACOX1 NM_004035.6 ?/. - c.1177C>T r.(?) p.(Arg393Trp)


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