Product Details

SNP ID

rs736523

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75591986 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACCCCTCCCTGTACAGGTGGAGGAT[A/G]TGCTGCCTATACTCAGCAGCTTTGG

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	2416	Missense Mutation	ATG,GTG	M853V	NP_001296171.1
XM_017025120.1	2416	Missense Mutation	ATG,GTG	M635V	XP_016880609.1
XM_017025121.1	2416	Missense Mutation	ATG,GTG	M630V	XP_016880610.1
XM_017025122.1	2416	Missense Mutation	ATG,GTG	M635V	XP_016880611.1
XM_017025123.1	2416	Missense Mutation	ATG,GTG	M635V	XP_016880612.1
XM_017025124.1	2416	Missense Mutation	ATG,GTG	M635V	XP_016880613.1
XM_017025125.1	2416	Missense Mutation	ATG,GTG	M635V	XP_016880614.1
XM_017025126.1	2416	Missense Mutation	ATG,GTG	M635V	XP_016880615.1
XM_017025127.1	2416	Missense Mutation	ATG,GTG	M406V	XP_016880616.1
XM_017025128.1	2416	Missense Mutation	ATG,GTG	M397V	XP_016880617.1
XM_017025129.1	2416	Missense Mutation	ATG,GTG	M114V	XP_016880618.1
XM_017025130.1	2416	Missense Mutation	ATG,GTG	M106V	XP_016880619.1
XM_017025131.1	2416	Missense Mutation	ATG,GTG	M71V	XP_016880620.1
XM_017025132.1	2416	UTR 5			XP_016880621.1
XM_017025133.1	2416	UTR 5			XP_016880622.1
XM_017025134.1	2416	UTR 5			XP_016880623.1
XM_017025135.1	2416	Intron			XP_016880624.1
XM_017025136.1	2416	Intron			XP_016880625.1
XM_017025137.1	2416	Intron			XP_016880626.1
XM_017025138.1	2416	Intron			XP_016880627.1
XM_017025139.1	2416	Intron			XP_016880628.1
XM_017025140.1	2416	Intron			XP_016880629.1
XM_017025141.1	2416	Missense Mutation	ATG,GTG	M635V	XP_016880630.1
XM_017025142.1	2416	Missense Mutation	ATG,GTG	M635V	XP_016880631.1
XM_017025143.1	2416	Intron			XP_016880632.1
XM_017025144.1	2416	UTR 5			XP_016880633.1

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