Product Details

SNP ID
rs142107935
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:1467255 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCCCACTCACCACAGCCAGGTGC[C/T]CGTTCTTGGCCTTGGTGATGAGCAG
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 3156 Missense Mutation GAG,GGG E1051G NP_001074248.1
NM_001080950.1 3156 Missense Mutation GAG,GGG E1032G NP_001074419.1
NM_033375.4 3156 Missense Mutation GAG,GGG E1016G NP_203693.3

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