Variant #0000333437 (NC_000023.10:g.23740077G>C, NM_001033583.2:c.482C>G (ACOT9))

Chromosome X
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.23740077G>C
DNA change (hg38) g.23721960G>C
Published as ACOT9(NM_001033583.2):c.482C>G (p.(Pro161Arg))
ISCN -
DB-ID ACOT9_000027
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) Retrieve
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     
ACOT9 NM_001033583.2 ?/. - c.482C>G r.(?) p.(Pro161Arg)
ACOT9 NM_001037171.1 ?/. - c.509C>G r.(?) p.(Pro170Arg)


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