Variant #0000575324 (NC_000023.10:g.23723695T>C, NM_001033583.2:c.923A>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.23723695T>C
DNA change (hg38) g.23705578T>C
Published as ACOT9(NM_001330259.1):c.743A>G (p.N248S)
ISCN -
DB-ID ACOT9_000033
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_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 2025-02-07 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.923A>G r.(?) p.(Asn308Ser)
ACOT9 NM_001037171.1 ?/. - c.950A>G r.(?) p.(Asn317Ser)


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