Product Details

SNP ID

rs147125759

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:46859491 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCCTCACCCAGCGTGGCCAGCAC[A/G]TGGCGAAGCTCAGCACCCATGACAG

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	558	Silent Mutation	CAC,CAT	H155H	NP_000249.1

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