Product Details

SNP ID
rs140900113
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:1468001 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCCTGGCTGACCGGTCAGGTTGGC[A/G]TAATCAATCCTCTGCTTGACTTTGG
Phenotype
MIM: 606538
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MYO1C PubMed Links

Gene Details

Gene
MYO1C
Gene Name
myosin IC
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080779.1 2887 Silent Mutation TAC,TAT Y961Y NP_001074248.1
NM_001080950.1 2887 Silent Mutation TAC,TAT Y942Y NP_001074419.1
NM_033375.4 2887 Silent Mutation TAC,TAT Y926Y NP_203693.3

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