Product Details

SNP ID
rs181668441
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:1468000 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACCCTGGCTGACCGGTCAGGTTGG[C/T]GTAATCAATCCTCTGCTTGACTTTG
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 2888 Missense Mutation ACC,GCC T962A NP_001074248.1
NM_001080950.1 2888 Missense Mutation ACC,GCC T943A NP_001074419.1
NM_033375.4 2888 Missense Mutation ACC,GCC T927A NP_203693.3

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