Variant #0000260491 (NC_000023.10:g.23754111G>A, NM_001033583.2:c.43C>T (ACOT9))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.23754111G>A
DNA change (hg38) g.23735994G>A
Published as ACOT9(NM_001037171.2):c.43C>T (p.Q15*)
ISCN -
DB-ID ACOT9_000030
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.43C>T r.(?) p.(Gln15Ter)
ACOT9 NM_001037171.1 -?/. - c.43C>T r.(?) p.(Gln15Ter)


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