Product Details

SNP ID

rs80252608

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75591193 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAGACACATCTTTGCCATCGTGGC[A/G]TCAGCCTATGACCTGGCTCAGAATA

Phenotype

Polymorphism

A/G, 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	2241	Silent Mutation	GCA,GCG	A794A	NP_001296171.1
XM_017025120.1	2241	Silent Mutation	GCA,GCG	A576A	XP_016880609.1
XM_017025121.1	2241	Silent Mutation	GCA,GCG	A576A	XP_016880610.1
XM_017025122.1	2241	Silent Mutation	GCA,GCG	A576A	XP_016880611.1
XM_017025123.1	2241	Silent Mutation	GCA,GCG	A576A	XP_016880612.1
XM_017025124.1	2241	Silent Mutation	GCA,GCG	A576A	XP_016880613.1
XM_017025125.1	2241	Silent Mutation	GCA,GCG	A576A	XP_016880614.1
XM_017025126.1	2241	Silent Mutation	GCA,GCG	A576A	XP_016880615.1
XM_017025127.1	2241	Silent Mutation	GCA,GCG	A347A	XP_016880616.1
XM_017025128.1	2241	Silent Mutation	GCA,GCG	A338A	XP_016880617.1
XM_017025129.1	2241	Silent Mutation	GCA,GCG	A55A	XP_016880618.1
XM_017025130.1	2241	Silent Mutation	GCA,GCG	A52A	XP_016880619.1
XM_017025131.1	2241	Silent Mutation	GCA,GCG	A17A	XP_016880620.1
XM_017025132.1	2241	UTR 5			XP_016880621.1
XM_017025133.1	2241	Intron			XP_016880622.1
XM_017025134.1	2241	UTR 5			XP_016880623.1
XM_017025135.1	2241	Intron			XP_016880624.1
XM_017025136.1	2241	Intron			XP_016880625.1
XM_017025137.1	2241	Intron			XP_016880626.1
XM_017025138.1	2241	Intron			XP_016880627.1
XM_017025139.1	2241	Intron			XP_016880628.1
XM_017025140.1	2241	Intron			XP_016880629.1
XM_017025141.1	2241	Silent Mutation	GCA,GCG	A576A	XP_016880630.1
XM_017025142.1	2241	Silent Mutation	GCA,GCG	A576A	XP_016880631.1
XM_017025143.1	2241	Intron			XP_016880632.1
XM_017025144.1	2241	UTR 5			XP_016880633.1

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