Product Details

SNP ID
rs143784817
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:47209508 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAGCCCCTGCACCAGCCCCTGCCC[C/T]AGCTCCTGAGGCTCCCAAGGAACCT
Phenotype
MIM: 160770
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MYL4 PubMed Links

Gene Details

Gene
MYL4
Gene Name
myosin light chain 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001002841.1 161 Missense Mutation CCA,CTA P29L NP_001002841.1
NM_002476.2 161 Missense Mutation CCA,CTA P29L NP_002467.1
XM_005257391.4 161 Missense Mutation CCA,CTA P29L XP_005257448.1
XM_011524839.2 161 Missense Mutation CCA,CTA P29L XP_011523141.2
XM_017024683.1 161 Missense Mutation CCA,CTA P29L XP_016880172.1
XM_017024684.1 161 Missense Mutation CCA,CTA P29L XP_016880173.1

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