Product Details

SNP ID

rs200459313

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:24057468 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGTTCTTGACGAAGACGCCGTAGC[A/G]GCCGCTGTCTTCACTGTTGACCTTC

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	4373	Missense Mutation			NP_689585.3

View Full Product Details