Product Details

SNP ID

rs17064579

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:2049989 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTTTCCTGCTCACCTCCTGCTACG[A/C]CTGTCTACCGTAACCAGTGAGACTT

Phenotype

MIM: 603509

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

MYOM2 PubMed Links

Gene Details

Gene

MYOM2

Gene Name

myomesin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003970.3		Intron			NP_003961.3
XM_006716237.1		Intron			XP_006716300.1

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