Product Details

SNP ID

rs2609433

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:70637479 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGTGCATGGTGTGTGTTTGTTGGG[G/T]GTTGTGGAGGGTATGTTTTTGAGTG

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		Intron			NP_114095.2
XM_006714056.3		Intron			XP_006714119.1

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