Product Details

SNP ID

rs202242697

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:1201747 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAGCAGGAGGAGGCCAGCTCCCGG[A/C]CGAAGTGGGACAACAAGGCGCAGTA

Phenotype

MIM: 608893

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

SLC6A19 PubMed Links

Gene Details

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	153	Missense Mutation	ACG,CCG	T33P	NP_001003841.1

View Full Product Details