Product Details

SNP ID

rs707710

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75588194 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCCGTTCCGACCGCGGGCAGGCGG[A/C]CAGGGCGAAACCGGCGGCCGAGCCT

Phenotype

Polymorphism

A/C, 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	650	Missense Mutation	GAC,GCC	D46A	NP_001296171.1
XM_017025120.1	650	Missense Mutation	GAC,GCC	D46A	XP_016880609.1
XM_017025121.1	650	Missense Mutation	GAC,GCC	D46A	XP_016880610.1
XM_017025122.1	650	Missense Mutation	GAC,GCC	D46A	XP_016880611.1
XM_017025123.1	650	Missense Mutation	GAC,GCC	D46A	XP_016880612.1
XM_017025124.1	650	Missense Mutation	GAC,GCC	D46A	XP_016880613.1
XM_017025125.1	650	Missense Mutation	GAC,GCC	D46A	XP_016880614.1
XM_017025126.1	650	Missense Mutation	GAC,GCC	D46A	XP_016880615.1
XM_017025127.1	650	Missense Mutation	GAC,GCC	D46A	XP_016880616.1
XM_017025128.1	650	Missense Mutation	ACA,CCA	T16P	XP_016880617.1
XM_017025129.1	650	Intron			XP_016880618.1
XM_017025130.1	650	Intron			XP_016880619.1
XM_017025131.1	650	Intron			XP_016880620.1
XM_017025132.1	650	Intron			XP_016880621.1
XM_017025133.1	650	Intron			XP_016880622.1
XM_017025134.1	650	Intron			XP_016880623.1
XM_017025135.1	650	Intron			XP_016880624.1
XM_017025136.1	650	Intron			XP_016880625.1
XM_017025137.1	650	Intron			XP_016880626.1
XM_017025138.1	650	Intron			XP_016880627.1
XM_017025139.1	650	Intron			XP_016880628.1
XM_017025140.1	650	Intron			XP_016880629.1
XM_017025141.1	650	Missense Mutation	GAC,GCC	D46A	XP_016880630.1
XM_017025142.1	650	Missense Mutation	GAC,GCC	D46A	XP_016880631.1
XM_017025143.1	650	Intron			XP_016880632.1
XM_017025144.1	650	UTR 5			XP_016880633.1

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