Variant #0000563127 (NC_000017.10:g.73944473C>A, NM_004035.6:c.1794G>T (ACOX1))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73944473C>A
DNA change (hg38) g.75948392C>A
Published as ACOX1(NM_001185039.1):c.1680G>T (p.L560=)
ISCN -
DB-ID ACOX1_000008
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) 0.00153 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-01-07 15:52:25 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TEN1 NM_001113324.2 -/. - c.-31126C>A r.(?) p.(=)
ACOX1 NM_004035.6 -/. - c.1794G>T r.(?) p.(Leu598=)


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