Product Details

SNP ID

rs148864919

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:128966364 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTCGGAAACCTTTCATCATCTATG[A/G]GGGAGACATCTACACCTATCAGGAT

Phenotype

MIM: 604196

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC27A6 PubMed Links

Gene Details

Gene

SLC27A6

Gene Name

solute carrier family 27 member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001017372.2	1062	Missense Mutation	GAG,GGG	E76G	NP_001017372.1
NM_001317984.1	1062	Missense Mutation	GAG,GGG	E76G	NP_001304913.1
NM_014031.4	1062	Missense Mutation	GAG,GGG	E76G	NP_054750.1

View Full Product Details