Product Details

SNP ID

rs820241

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75590103 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTCCCTGAGGGAGCTGTGGGAACC[C/G]GAGGATGAGGACGAGGCGGTGCTGG

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	1905	Silent Mutation	CCC,CCG	P682P	NP_001296171.1
XM_017025120.1	1905	Silent Mutation	CCC,CCG	P464P	XP_016880609.1
XM_017025121.1	1905	Silent Mutation	CCC,CCG	P464P	XP_016880610.1
XM_017025122.1	1905	Silent Mutation	CCC,CCG	P464P	XP_016880611.1
XM_017025123.1	1905	Silent Mutation	CCC,CCG	P464P	XP_016880612.1
XM_017025124.1	1905	Silent Mutation	CCC,CCG	P464P	XP_016880613.1
XM_017025125.1	1905	Silent Mutation	CCC,CCG	P464P	XP_016880614.1
XM_017025126.1	1905	Silent Mutation	CCC,CCG	P464P	XP_016880615.1
XM_017025127.1	1905	Intron			XP_016880616.1
XM_017025128.1	1905	Intron			XP_016880617.1
XM_017025129.1	1905	Intron			XP_016880618.1
XM_017025130.1	1905	Intron			XP_016880619.1
XM_017025131.1	1905	Intron			XP_016880620.1
XM_017025132.1	1905	Intron			XP_016880621.1
XM_017025133.1	1905	Intron			XP_016880622.1
XM_017025134.1	1905	Intron			XP_016880623.1
XM_017025135.1	1905	Intron			XP_016880624.1
XM_017025136.1	1905	Intron			XP_016880625.1
XM_017025137.1	1905	Intron			XP_016880626.1
XM_017025138.1	1905	Intron			XP_016880627.1
XM_017025139.1	1905	Intron			XP_016880628.1
XM_017025140.1	1905	Intron			XP_016880629.1
XM_017025141.1	1905	Silent Mutation	CCC,CCG	P464P	XP_016880630.1
XM_017025142.1	1905	Silent Mutation	CCC,CCG	P464P	XP_016880631.1
XM_017025143.1	1905	Intron			XP_016880632.1
XM_017025144.1	1905	UTR 5			XP_016880633.1

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