Product Details

SNP ID

rs12592989

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:59138351 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCCCTGCTGGGGGAGGCCGACTGG[C/T]TGTTTGTCTCCTGACCCTGTGGAGA

Phenotype

MIM: 601479

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYO1E PubMed Links

Gene Details

Gene

MYO1E

Gene Name

myosin IE

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004998.3	3469	Missense Mutation	ACC,GCC	T1033A	NP_004989.2

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