Product Details

SNP ID

rs10079058

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:16664131 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AACTGAAGGGCACGCAGGCCTCCCT[C/G]TACGTTCTGTTGCAACTTTCTCTGA

Phenotype

MIM: 601481

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

MYO10 PubMed Links

Gene Details

Gene

MYO10

Gene Name

myosin X

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_012334.2	9206	UTR 3			NP_036466.2
XM_005248306.4	9206	Intron			XP_005248363.1
XM_005248307.2	9206	Intron			XP_005248364.1
XM_006714475.2	9206	Intron			XP_006714538.1
XM_011514046.2	9206	Intron			XP_011512348.1

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