Product Details

SNP ID

rs142303290

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:223172 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CACAGAGGGACTCGAAGATGGCCAC[A/G]AACAGGAGGCACATGCCACTGGCCG

Phenotype

MIM: 603080 MIM: 615097

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SLC6A12 PubMed Links

Additional Information

For this assay, SNP(s) [rs2289954] 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

SLC6A12

Gene Name

solute carrier family 6 member 12

There are no transcripts associated with this gene.

Gene

SLC6A13

Gene Name

solute carrier family 6 member 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001190997.2	1532	Silent Mutation	TTC,TTT	F366F	NP_001177926.1
NM_001243392.1	1532	Intron			NP_001230321.1
NM_016615.4	1532	Silent Mutation	TTC,TTT	F458F	NP_057699.2
XM_006719008.3	1532	Silent Mutation	TTC,TTT	F215F	XP_006719071.1
XM_011521012.2	1532	Silent Mutation	TTC,TTT	F339F	XP_011519314.1
XM_011521013.1	1532	Silent Mutation	TTC,TTT	F296F	XP_011519315.1
XM_011521014.1	1532	Silent Mutation	TTC,TTT	F296F	XP_011519316.1
XM_017019842.1	1532	Silent Mutation	TTC,TTT	F301F	XP_016875331.1
XM_017019843.1	1532	Silent Mutation	TTC,TTT	F298F	XP_016875332.1
XM_017019844.1	1532	Intron			XP_016875333.1
XM_017019845.1	1532	Silent Mutation	TTC,TTT	F215F	XP_016875334.1
XM_017019846.1	1532	Intron			XP_016875335.1
XM_017019847.1	1532	Intron			XP_016875336.1

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