Product Details

SNP ID

rs726449

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.13:108499141 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTTAATTGAGATCAAACATTTATA[C/T]TCAACTTGCCTGTTTTAAGCATGGA

Phenotype

MIM: 615479

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYO16 PubMed Links

Gene Details

Gene

MYO16

Gene Name

myosin XVI

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001198950.1		Intron			NP_001185879.1
NM_015011.1		Intron			NP_055826.1
XM_011521062.1		Intron			XP_011519364.1

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