Product Details

SNP ID
rs202141423
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:46859510 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCACGTGGCGAAGCTCAGCACCC[A/G]TGACAGTGCCATTGCCCTCCTTGTC
Phenotype
MIM: 160790
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
MYL3 PubMed Links

Gene Details

Gene
MYL3
Gene Name
myosin light chain 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000258.2 539 Missense Mutation ACG,ATG T149M NP_000249.1

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