Product Details

SNP ID
rs10104822
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:2046483 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCGTGGCCCTACCGGTGACCCGGGC[A/G]AGTCATATTTCCCTGGGGACGGTCT
Phenotype
MIM: 603509
Polymorphism
A/G, Transition 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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