Product Details

SNP ID

rs149519721

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:81078328 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTACAAGACCCACTTCGCAGCCTCG[A/G]TGACCGACCCCGAGAGGTTCTGGGG

Phenotype

MIM: 614356

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ACSS3 PubMed Links

Gene Details

Gene

ACSS3

Gene Name

acyl-CoA synthetase short-chain family member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005269150.2	311	Missense Mutation	ATG,GTG	M70V	XP_005269207.1
XM_005269151.4	311	Missense Mutation	ATG,GTG	M70V	XP_005269208.1
XM_011538740.2	311	Intron			XP_011537042.1

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