Product Details

SNP ID

rs9368895

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:35945319 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATTTCTCTGGCTTTTCTAGCTAGAC[A/C]GGATTTCATGACCAACCATTTAAAA

Phenotype

MIM: 608480

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SLC26A8 PubMed Links

Additional Information

For this assay, SNP(s) [rs117475331,rs117903426] 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

SLC26A8

Gene Name

solute carrier family 26 member 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001193476.1		Intron			NP_001180405.1
NM_052961.3		Intron			NP_443193.1
NM_138718.2		Intron			NP_619732.2
XM_011514294.2		Intron			XP_011512596.1
XM_017010235.1		Intron			XP_016865724.1

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