Variant #0000984611 (NC_000023.10:g.23731271G>A, NM_001033583.2:c.616C>T (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.23731271G>A
DNA change (hg38) -
Published as ACOT9(NM_001037171.2):c.643C>T (p.(Arg215Cys))
ISCN -
DB-ID ACOT9_000043
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACOT9 NM_001033583.2 ?/. - c.616C>T r.(?) p.(Arg206Cys)
ACOT9 NM_001037171.1 ?/. - c.643C>T r.(?) p.(Arg215Cys)


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