Product Details

SNP ID

rs201761830

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:24057428 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAACACACTGATGGTGACCTGGCCC[A/G]TCTCGGAGCCATACTTGTTCTTGAC

Phenotype

MIM: 616832

Polymorphism

A/G, 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	4413	Missense Mutation	ACG,ATG	T1417M	NP_689585.3

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