Product Details

SNP ID

rs4789219

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75590479 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGAGCCAGCCCTCCTTGTAGCCTGC[C/G]CATTACTTGACAGCTCAGCCCCCAT

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

MYO15B PubMed Links

Gene Details

Gene

MYO15B

Gene Name

myosin XVB

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001309242.1		Intron			NP_001296171.1
XM_017025120.1		Intron			XP_016880609.1
XM_017025121.1		Intron			XP_016880610.1
XM_017025122.1		Intron			XP_016880611.1
XM_017025123.1		Intron			XP_016880612.1
XM_017025124.1		Intron			XP_016880613.1
XM_017025125.1		Intron			XP_016880614.1
XM_017025126.1		Intron			XP_016880615.1
XM_017025127.1		Intron			XP_016880616.1
XM_017025128.1		Intron			XP_016880617.1
XM_017025129.1		Intron			XP_016880618.1
XM_017025130.1		Intron			XP_016880619.1
XM_017025131.1		Intron			XP_016880620.1
XM_017025132.1		Intron			XP_016880621.1
XM_017025133.1		Intron			XP_016880622.1
XM_017025134.1		Intron			XP_016880623.1
XM_017025135.1		Intron			XP_016880624.1
XM_017025136.1		Intron			XP_016880625.1
XM_017025137.1		Intron			XP_016880626.1
XM_017025138.1		Intron			XP_016880627.1
XM_017025139.1		Intron			XP_016880628.1
XM_017025140.1		Intron			XP_016880629.1
XM_017025141.1		Intron			XP_016880630.1
XM_017025142.1		Intron			XP_016880631.1
XM_017025143.1		Intron			XP_016880632.1
XM_017025144.1		Intron			XP_016880633.1

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