Product Details

SNP ID

rs144423836

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:128345436 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGGGCCTATGGCTGGGCATGGCCA[A/G]GCTCGGTGTGGAGGCAGCCCTCATC

Phenotype

MIM: 604194

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC27A4 PubMed Links

Gene Details

Gene

SLC27A4

Gene Name

solute carrier family 27 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005094.3	601	Missense Mutation	AAG,AGG	K148R	NP_005085.2
XM_017014222.1	601	Missense Mutation	AAG,AGG	K148R	XP_016869711.1

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