Product Details

SNP ID

rs7143253

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:52739379 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCACTTTAGATAAATTCAAAAGTAC[G/T]CATTTCTTTAATTGATTTTCTTCTT

Phenotype

MIM: 615814

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

STYX PubMed Links

Additional Information

For this assay, SNP(s) [rs114955522] 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

STYX

Gene Name

serine/threonine/tyrosine interacting protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130701.1		Intron			NP_001124173.1
NM_145251.3		Intron			NP_660294.1
XM_006720242.3		Intron			XP_006720305.1
XM_011537108.2		Intron			XP_011535410.1
XM_011537109.2		Intron			XP_011535411.1

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