Product Details

SNP ID

rs2097844

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:50353333 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTTATTTTAACATCTGCTGAAAAAG[A/G]AAGTGGTATCTGAGTCCAGAACAGA

Phenotype

MIM: 608125

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

XYLT2 PubMed Links

Additional Information

For this assay, SNP(s) [rs72832451] 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

XYLT2

Gene Name

xylosyltransferase 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022167.3		Intron			NP_071450.2
XM_005257572.4		Intron			XP_005257629.1

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