Product Details

SNP ID

rs146902785

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:128345349 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAAGCAGTGTAGCCAACTTCCTGC[A/T]GGCCCGGGGCCTGGCCTCGGGCGAT

Phenotype

MIM: 604194

Polymorphism

A/T, Transversion 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	514	Missense Mutation	CAG,CTG	Q119L	NP_005085.2
XM_017014222.1	514	Missense Mutation	CAG,CTG	Q119L	XP_016869711.1

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