Product Details

SNP ID
rs147835827
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:1468048 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGGCGTCCTCCACGATGACGACGG[C/T]GTTGGGCGTGAGCAGCAGCTGCCGG
Phenotype
MIM: 606538
Polymorphism
C/T, 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 2840 Missense Mutation ACC,GCC T946A NP_001074248.1
NM_001080950.1 2840 Missense Mutation ACC,GCC T927A NP_001074419.1
NM_033375.4 2840 Missense Mutation ACC,GCC T911A NP_203693.3

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