Product Details

SNP ID

rs6992142

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:2049511 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGTACCCTGGAGATCTGAACTATGA[C/G]AAATTCATCTCCGAGCAGCCCTTGG

Phenotype

MIM: 603509

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

MYOM2 PubMed Links

Additional Information

For this assay, SNP(s) [rs77124651] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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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