Product Details

SNP ID

rs117785251

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75591675 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAAAGATCATGCAGTTCCTAAGCA[G/T]CCTGGAGCAGGATCAGACGGGGAAC

Phenotype

Polymorphism

G/T, 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	2369	Missense Mutation	AGC,ATC	S837I	NP_001296171.1
XM_017025120.1	2369	Missense Mutation	AGC,ATC	S619I	XP_016880609.1
XM_017025121.1	2369	Missense Mutation	AGC,ATC	S614I	XP_016880610.1
XM_017025122.1	2369	Missense Mutation	AGC,ATC	S619I	XP_016880611.1
XM_017025123.1	2369	Missense Mutation	AGC,ATC	S619I	XP_016880612.1
XM_017025124.1	2369	Missense Mutation	AGC,ATC	S619I	XP_016880613.1
XM_017025125.1	2369	Missense Mutation	AGC,ATC	S619I	XP_016880614.1
XM_017025126.1	2369	Missense Mutation	AGC,ATC	S619I	XP_016880615.1
XM_017025127.1	2369	Missense Mutation	AGC,ATC	S390I	XP_016880616.1
XM_017025128.1	2369	Missense Mutation	AGC,ATC	S381I	XP_016880617.1
XM_017025129.1	2369	Missense Mutation	AGC,ATC	S98I	XP_016880618.1
XM_017025130.1	2369	Missense Mutation	AGC,ATC	S90I	XP_016880619.1
XM_017025131.1	2369	Missense Mutation	AGC,ATC	S55I	XP_016880620.1
XM_017025132.1	2369	UTR 5			XP_016880621.1
XM_017025133.1	2369	UTR 5			XP_016880622.1
XM_017025134.1	2369	UTR 5			XP_016880623.1
XM_017025135.1	2369	Intron			XP_016880624.1
XM_017025136.1	2369	Intron			XP_016880625.1
XM_017025137.1	2369	Intron			XP_016880626.1
XM_017025138.1	2369	Intron			XP_016880627.1
XM_017025139.1	2369	Intron			XP_016880628.1
XM_017025140.1	2369	Intron			XP_016880629.1
XM_017025141.1	2369	Missense Mutation	AGC,ATC	S619I	XP_016880630.1
XM_017025142.1	2369	Missense Mutation	AGC,ATC	S619I	XP_016880631.1
XM_017025143.1	2369	Intron			XP_016880632.1
XM_017025144.1	2369	UTR 5			XP_016880633.1

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