Product Details

SNP ID
rs200544334
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:59138354 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGCTGGGGGAGGCCGACTGGTTG[G/T]TTGTCTCCTGACCCTGTGGAGAGAG
Phenotype
MIM: 601479
Polymorphism
G/T, Transversion 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 3466 Missense Mutation ACA,CCA T1032P NP_004989.2

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