Product Details

SNP ID

rs112448746

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:59652896 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATAAAACCTCCCAGCAGGACGCAG[A/G]AGCCACTAAAATAAAATGCAATATC

Phenotype

MIM: 614242

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC16A9 PubMed Links

Additional Information

For this assay, SNP(s) [rs11006655] 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

SLC16A9

Gene Name

solute carrier family 16 member 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001323977.1	1808	Missense Mutation	TCC,TTC	S382F	NP_001310906.1
NM_001323978.1	1808	Missense Mutation	TCC,TTC	S382F	NP_001310907.1
NM_001323979.1	1808	Missense Mutation	TCC,TTC	S382F	NP_001310908.1
NM_001323980.1	1808	Missense Mutation	TCC,TTC	S382F	NP_001310909.1
NM_001323981.1	1808	Missense Mutation	TCC,TTC	S469F	NP_001310910.1
NM_194298.2	1808	Missense Mutation	TCC,TTC	S469F	NP_919274.1
XM_017015883.1	1808	Missense Mutation	TCC,TTC	S511F	XP_016871372.1
XM_017015884.1	1808	Missense Mutation	TCC,TTC	S469F	XP_016871373.1

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