Product Details

SNP ID

rs2291379

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:146255419 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTGCATCCATGACCTTTATATTTT[A/C]ATTTATTCATGAAAGCAATATGATT

Phenotype

MIM: 611459

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SLC10A7 PubMed Links

Additional Information

For this assay, SNP(s) [rs79938523] 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

SLC10A7

Gene Name

solute carrier family 10 member 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001029998.5	2421	UTR 3			NP_001025169.1
NM_001300842.2	2421	UTR 3			NP_001287771.1
NM_001317816.1	2421	UTR 3			NP_001304745.1
NM_001317817.1	2421	Intron			NP_001304746.1
NM_001317818.1	2421	Intron			NP_001304747.1
NM_032128.4	2421	Intron			NP_115504.1
XM_011532311.2	2421	UTR 3			XP_011530613.1
XM_011532313.2	2421	UTR 3			XP_011530615.1
XM_011532314.2	2421	UTR 3			XP_011530616.1
XM_017008689.1	2421	Intron			XP_016864178.1
XM_017008690.1	2421	Intron			XP_016864179.1
XM_017008691.1	2421	Intron			XP_016864180.1
XM_017008692.1	2421	Intron			XP_016864181.1

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