Product Details

SNP ID

rs2158468

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:15051947 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGACACAGGAAGTTTTTGGGGGCGG[A/G]GTGGGGGACATTGTGGGGTAGGCTC

Phenotype

MIM: 605848

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

CASP14 PubMed Links

Additional Information

For this assay, SNP(s) [rs78781651] 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

CASP14

Gene Name

caspase 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012114.2		Intron			NP_036246.1
XM_011527861.1		Intron			XP_011526163.1

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