Product Details

SNP ID

rs144052642

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:70628161 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGTCCTATTTTCATTAAGTTGTAT[C/T]ATCATAATAGCTGAGAGTTCATTTG

Phenotype

MIM: 606585

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ENAM PubMed Links

Additional Information

For this assay, SNP(s) [rs566763661] 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

ENAM

Gene Name

enamelin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031889.2	691	Intron			NP_114095.2
XM_006714056.3	691	UTR 5			XP_006714119.1

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