Product Details

SNP ID

rs202157618

Assay Type

Functionally tested

NCBI dbSNP Submissions

18

Location

Chr.1:24057541 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCCCTCACTTCCATGCGGTATCG[G/T]TCAAGGAAGGTGACAGGCTGGTCAT

Phenotype

MIM: 616832

Polymorphism

G/T, Transversion 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	4300	Silent Mutation	GAG,GAT	E1379D	NP_689585.3

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