Product Details

SNP ID

rs8071258

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:6685287 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAGGGCCTAGATAGCCCACTGTGG[C/T]CCCCAGAGCGCCATCACTGCCCATA

Phenotype

MIM: 608305

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC13A5 PubMed Links

Additional Information

For this assay, SNP(s) [rs76821126] are located under a probe 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

SLC13A5

Gene Name

solute carrier family 13 member 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143838.2	2586	UTR 3			NP_001137310.1
NM_001284509.1	2586	UTR 3			NP_001271438.1
NM_001284510.1	2586	UTR 3			NP_001271439.1
NM_177550.4	2586	UTR 3			NP_808218.1
XM_011523795.2	2586	Intron			XP_011522097.1

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