Variant #0000325629 (NC_000017.10:g.73996233G>A, NM_004035.6:c.-21079C>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.73996233G>A
DNA change (hg38) g.76000152G>A
Published as TEN1(NM_001113324.2):c.262G>A (p.(Val88Met))
ISCN -
DB-ID TEN1_000001
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) 0.0007 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.262G>A r.(?) p.(Val88Met)
CDK3 NM_001258.2 ?/. - c.-830G>A r.(?) p.(=)
ACOX1 NM_004035.6 ?/. - c.-21079C>T r.(?) p.(=)
TEN1-CDK3 NR_037709.1 ?/. - n.563G>A r.(?) -


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