Product Details

SNP ID
rs1143658
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:3067544 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGGGTCTCCCCACACGTTGCAAGT[G/C]AGATTAAGGGCCTGCAAGACAGGTT
Phenotype
MIM: 603508
Polymorphism
G/C, Transversion substitution
Allele Nomenclature
Literature Links
MYOM1 PubMed Links

Gene Details

Gene
MYOM1
Gene Name
myomesin 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003803.3 4837 Silent Mutation CTC,CTG L1592L NP_003794.3
NM_019856.1 4837 Silent Mutation CTC,CTG L1496L NP_062830.1
XM_017026062.1 4837 Silent Mutation CTC,CTG L1580L XP_016881551.1

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