Product Details

SNP ID

rs147655466

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75591176 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAACCTTCTCATCTCCCTCAGACAC[A/G]TCTTTGCCATCGTGGCATCAGCCTA

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	2224	Missense Mutation	ATC,GTC	I789V	NP_001296171.1
XM_017025120.1	2224	Missense Mutation	ATC,GTC	I571V	XP_016880609.1
XM_017025121.1	2224	Missense Mutation	ATC,GTC	I571V	XP_016880610.1
XM_017025122.1	2224	Missense Mutation	ATC,GTC	I571V	XP_016880611.1
XM_017025123.1	2224	Missense Mutation	ATC,GTC	I571V	XP_016880612.1
XM_017025124.1	2224	Missense Mutation	ATC,GTC	I571V	XP_016880613.1
XM_017025125.1	2224	Missense Mutation	ATC,GTC	I571V	XP_016880614.1
XM_017025126.1	2224	Missense Mutation	ATC,GTC	I571V	XP_016880615.1
XM_017025127.1	2224	Missense Mutation	ATC,GTC	I342V	XP_016880616.1
XM_017025128.1	2224	Missense Mutation	ATC,GTC	I333V	XP_016880617.1
XM_017025129.1	2224	Missense Mutation	ATC,GTC	I50V	XP_016880618.1
XM_017025130.1	2224	Missense Mutation	ATC,GTC	I47V	XP_016880619.1
XM_017025131.1	2224	Missense Mutation	ATC,GTC	I12V	XP_016880620.1
XM_017025132.1	2224	UTR 5			XP_016880621.1
XM_017025133.1	2224	Intron			XP_016880622.1
XM_017025134.1	2224	UTR 5			XP_016880623.1
XM_017025135.1	2224	Intron			XP_016880624.1
XM_017025136.1	2224	Intron			XP_016880625.1
XM_017025137.1	2224	Intron			XP_016880626.1
XM_017025138.1	2224	Intron			XP_016880627.1
XM_017025139.1	2224	Intron			XP_016880628.1
XM_017025140.1	2224	Intron			XP_016880629.1
XM_017025141.1	2224	Missense Mutation	ATC,GTC	I571V	XP_016880630.1
XM_017025142.1	2224	Missense Mutation	ATC,GTC	I571V	XP_016880631.1
XM_017025143.1	2224	Intron			XP_016880632.1
XM_017025144.1	2224	UTR 5			XP_016880633.1

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