Product Details

SNP ID

rs11568634

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.11:62979488 on Build GRCh38

Set Membership

DME Validated Inventoried

Context Sequence [VIC/FAM]

ATTCTCCCATTAGGCTCCCACTCAC[C/T]GGATCATTGTGGGATACAGTTCCCC

Phenotype

MIM: 607582

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLC22A6 PubMed Links

Additional Information

For this assay, SNP(s) [rs201686570] 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

SLC22A6

Gene Name

solute carrier family 22 member 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004790.4	1694	Missense Mutation	CAG,CGG	Q454R	NP_004781.2
NM_153276.2	1694	Missense Mutation	CAG,CGG	Q454R	NP_695008.1
NM_153277.2	1694	Missense Mutation	CAC,CGC	H454R	NP_695009.1
NM_153278.2	1694	Missense Mutation	CAC,CGC	H454R	NP_695010.1
XM_017018562.1	1694	Missense Mutation	CAG,CGG	Q455R	XP_016874051.1

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