Product Details

SNP ID

rs16940182

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:109395294 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAAAAATACATGAGATCTTACTCTA[C/T]TTATTGAATTGAATTATTTAGTATT

Phenotype

MIM: 614636

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MYO1H PubMed Links

Gene Details

Gene

MYO1H

Gene Name

myosin IH

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001101421.3		Intron			NP_001094891.3
XM_011538223.2		Intron			XP_011536525.1
XM_017019207.1		Intron			XP_016874696.1

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