Product Details

SNP ID

rs28712717

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:2409955 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCAGAGATTCTGAGCACTTTTTTT[C/T]TTTTTCCTTTCAGGCAGAGTCTCAC

Phenotype

MIM: 610129

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CHST12 PubMed Links

Additional Information

For this assay, SNP(s) [rs77867789] 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

CHST12

Gene Name

carbohydrate (chondroitin 4) sulfotransferase 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243794.1		Intron			NP_001230723.1
NM_001243795.1		Intron			NP_001230724.1
NM_018641.4		Intron			NP_061111.1
XM_011515443.2		Intron			XP_011513745.1
XM_011515444.2		Intron			XP_011513746.1

View Full Product Details