Product Details

SNP ID

rs4149432

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:108378869 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTTTGAGTGTGTGAGCTAGAAAGG[G/T]GATCCTGAGTCTGATTTGGGAAAGA

Phenotype

MIM: 608357

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

SULT1C4 PubMed Links

Additional Information

For this assay, SNP(s) [rs41519947] are located under a probe 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

SULT1C4

Gene Name

sulfotransferase family 1C member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321770.1		Intron			NP_001308699.1
NM_006588.3		Intron			NP_006579.2
XM_017003807.1		Intron			XP_016859296.1

View Full Product Details