Product Details

SNP ID
rs1463395
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:46859905 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGAGTTTGCTGCCCTGAGCCACCA[C/T]GGAGGGCTCTGTCCAGAACCCCTTG
Phenotype
MIM: 160790
Polymorphism
C/T, 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 Intron NP_000249.1

View Full Product Details