Product Details

SNP ID

rs146707213

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:23705845 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCATTAGAGGGTAAAACTCGACTCC[A/G]AAAACTTATAGTCCTGTACAAATGA

Phenotype

MIM: 300862

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ACOT9 PubMed Links

Gene Details

Gene

ACOT9

Gene Name

acyl-CoA thioesterase 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001033583.2	1002	Missense Mutation	CGG,TGG	R277W	NP_001028755.2
NM_001037171.1	1002	Missense Mutation	CGG,TGG	R286W	NP_001032248.1
XM_005274472.2	1002	Missense Mutation	CGG,TGG	R217W	XP_005274529.1

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