Product Details

SNP ID

rs7540491

Assay Type

Functionally tested

NCBI dbSNP Submissions

64

Location

Chr.1:24057329 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TACAGGTTGTCCCTACTGGTCCATG[C/T]AGACTAGACTCAGACTGTGCCTGGA

Phenotype

MIM: 616832

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYOM3 PubMed Links

Gene Details

Gene

MYOM3

Gene Name

myomesin 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152372.3	4512	UTR 3			NP_689585.3

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