Product Details

SNP ID
rs2230164
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:3067280 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCTCCGGTCACTTGGCCTTCTTGCC[A/G]CCTTTCAGGGACTCCAAGGCGGCCA
Phenotype
MIM: 603508
Polymorphism
A/G, Transition 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 5101 Silent Mutation GGC,GGT G1680G NP_003794.3
NM_019856.1 5101 Silent Mutation GGC,GGT G1584G NP_062830.1
XM_017026062.1 5101 Silent Mutation GGC,GGT G1668G XP_016881551.1

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