Product Details

SNP ID

rs10999771

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:71322154 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCTCCCCGCCCCCCACCATCCCAGT[C/T]TCCCTCCTTAGAGACAGCCACTGTT

Phenotype

MIM: 612373

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC29A3 PubMed Links

Additional Information

For this assay, SNP(s) [rs78041015,rs78130441] 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

SLC29A3

Gene Name

solute carrier family 29 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001174098.1		Intron			NP_001167569.1
NM_018344.5		Intron			NP_060814.4
XM_006717910.3		Intron			XP_006717973.1
XM_017016377.1		Intron			XP_016871866.1
XM_017016378.1		Intron			XP_016871867.1

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