Product Details

SNP ID

rs149753564

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:1225604 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCGTGGGACTGGGGAACATTTGG[C/G]GGTTCCCATACCTGTGCCAGACCTA

Phenotype

MIM: 610300 MIM: 608893

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

SLC6A18 PubMed Links

Gene Details

Gene

SLC6A18

Gene Name

solute carrier family 6 member 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182632.2	250	Missense Mutation	CGG,GGG	R43G	NP_872438.2

Gene

SLC6A19

Gene Name

solute carrier family 6 member 19

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001003841.2	250	Intron			NP_001003841.1

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