Variant #0000575326 (NC_000023.10:g.23731321T>C, NM_001033583.2:c.566A>G (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.23731321T>C
DNA change (hg38) g.23713204T>C
Published as ACOT9(NM_001033583.2):c.566A>G (p.(His189Arg)), ACOT9(NM_001037171.2):c.593A>G (p.H198R), ACOT9(NM_001330259.1):c.386A>G (p.H129R)
ISCN -
DB-ID ACOT9_000026 See all 4 reported entries
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) 0.00298 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 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.566A>G r.(?) p.(His189Arg)
ACOT9 NM_001037171.1 -?/. - c.593A>G r.(?) p.(His198Arg)


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