Product Details

SNP ID
rs150224436
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:101616233 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGGAAACTTACACATCGGCCTTGA[C/T]GAAACCTTTCCCTTCAGTGTCGAAC
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
MYL10 PubMed Links

Gene Details

Gene
MYL10
Gene Name
myosin light chain 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_138403.4 418 Missense Mutation NP_612412.2
XM_017012793.1 418 Missense Mutation XP_016868282.1

View Full Product Details