Product Details

SNP ID

rs17111008

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.5:150195230 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTTCGTGATAAGGAGCTGTATCTG[A/C]CTGCCGATGATCACTGCACTTTCAG

Phenotype

MIM: 606205

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SLC6A7 PubMed Links

Additional Information

For this assay, SNP(s) [rs138122237,rs75427098] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

SLC6A7

Gene Name

solute carrier family 6 member 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014228.4	780	Intron			NP_055043.2
XM_017009767.1	780	Intron			XP_016865256.1
XM_017009768.1	780	Intron			XP_016865257.1
XM_017009769.1	780	UTR 5			XP_016865258.1
XM_017009770.1	780	Intron			XP_016865259.1

View Full Product Details