Product Details

SNP ID

rs1995967

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.13:31203468 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAGCAGTGTGAATTCGAAGGAGGTG[C/T]TTTGACCCCTTTGGTAACTTCCTGC

Phenotype

MIM: 610308

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

B3GLCT PubMed Links

Additional Information

For this assay, SNP(s) [rs77531102] 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

B3GLCT

Gene Name

beta 3-glucosyltransferase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_194318.3		Intron			NP_919299.3
XM_006719768.3		Intron			XP_006719831.1
XM_011534936.1		Intron			XP_011533238.1
XM_011534938.2		Intron			XP_011533240.1
XM_017020395.1		Intron			XP_016875884.1

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