Product Details

SNP ID

rs2609429

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:70632659 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATTCCTTTGGTTGCAGATGATGCG[G/T]TATAATCAATTCAACTTTATGAACG

Phenotype

MIM: 606585

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ENAM PubMed Links

Gene Details

Gene

ENAM

Gene Name

enamelin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031889.2	2207	Silent Mutation	CGG,CGT	R59R	NP_114095.2
XM_006714056.3	2207	Silent Mutation	CGG,CGT	R59R	XP_006714119.1

View Full Product Details