Product Details

SNP ID

rs150994609

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:101157358 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTTGAAAGCAGGATTATCAGTTCCA[C/T]CATCTTCCACTGGATGTGATTTATA

Phenotype

MIM: 608044

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC5A8 PubMed Links

Gene Details

Gene

SLC5A8

Gene Name

solute carrier family 5 member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145913.3	2144	Missense Mutation	GAT,GGT	D585G	NP_666018.3
XM_017018910.1	2144	Intron			XP_016874399.1

View Full Product Details