Product Details

SNP ID

rs1789321

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:63268494 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGAGAAGTCAATGTTCCAGCAAAGC[A/C]AACCATTCAGAGCCACATGAGTAAA

Phenotype

MIM: 607580

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

SLC22A10 PubMed Links

Additional Information

For this assay, SNP(s) [rs77193437] 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

SLC22A10

Gene Name

solute carrier family 22 member 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039752.3	238	Intron			NP_001034841.3
XM_011545016.2	238	UTR 5			XP_011543318.1
XM_017017699.1	238	Intron			XP_016873188.1
XM_017017700.1	238	Intron			XP_016873189.1
XM_017017701.1	238	UTR 5			XP_016873190.1
XM_017017702.1	238	UTR 5			XP_016873191.1
XM_017017703.1	238	Intron			XP_016873192.1
XM_017017704.1	238	Intron			XP_016873193.1

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