All transcript variants in gene ACOT9

Information The variants shown are described using the NM_001033583.2 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. - c.482C>G VUS r.(?) p.(Pro161Arg) g.23740077G>C - ACOT9(NM_001033583.2):c.482C>G (p.(Pro161Arg), p.(Pro170Arg)) - ACOT9_000027 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL
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