Product Details

SNP ID

rs28488097

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75590046 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACCCCGACTCTCCTTGGAGACCCG[C/T]CTGCAGCAGGAGGGAGACCCGGGCC

Phenotype

Polymorphism

C/T, Transition 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	1848	Silent Mutation	CGC,CGT	R663R	NP_001296171.1
XM_017025120.1	1848	Silent Mutation	CGC,CGT	R445R	XP_016880609.1
XM_017025121.1	1848	Silent Mutation	CGC,CGT	R445R	XP_016880610.1
XM_017025122.1	1848	Silent Mutation	CGC,CGT	R445R	XP_016880611.1
XM_017025123.1	1848	Silent Mutation	CGC,CGT	R445R	XP_016880612.1
XM_017025124.1	1848	Silent Mutation	CGC,CGT	R445R	XP_016880613.1
XM_017025125.1	1848	Silent Mutation	CGC,CGT	R445R	XP_016880614.1
XM_017025126.1	1848	Silent Mutation	CGC,CGT	R445R	XP_016880615.1
XM_017025127.1	1848	Intron			XP_016880616.1
XM_017025128.1	1848	Intron			XP_016880617.1
XM_017025129.1	1848	Intron			XP_016880618.1
XM_017025130.1	1848	Intron			XP_016880619.1
XM_017025131.1	1848	Intron			XP_016880620.1
XM_017025132.1	1848	Intron			XP_016880621.1
XM_017025133.1	1848	Intron			XP_016880622.1
XM_017025134.1	1848	Intron			XP_016880623.1
XM_017025135.1	1848	Intron			XP_016880624.1
XM_017025136.1	1848	Intron			XP_016880625.1
XM_017025137.1	1848	Intron			XP_016880626.1
XM_017025138.1	1848	Intron			XP_016880627.1
XM_017025139.1	1848	Intron			XP_016880628.1
XM_017025140.1	1848	Intron			XP_016880629.1
XM_017025141.1	1848	Silent Mutation	CGC,CGT	R445R	XP_016880630.1
XM_017025142.1	1848	Silent Mutation	CGC,CGT	R445R	XP_016880631.1
XM_017025143.1	1848	Intron			XP_016880632.1
XM_017025144.1	1848	UTR 5			XP_016880633.1

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