Product Details

SNP ID

rs1869575

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75588702 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACGGCCTGGACAGCGACTGGCCCCA[A/C]GCAGATACCCGGGGCCGGGAAGGGT

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	1158	Missense Mutation	CAA,CAC	Q215H	NP_001296171.1
XM_017025120.1	1158	Missense Mutation	CAA,CAC	Q215H	XP_016880609.1
XM_017025121.1	1158	Missense Mutation	CAA,CAC	Q215H	XP_016880610.1
XM_017025122.1	1158	Missense Mutation	CAA,CAC	Q215H	XP_016880611.1
XM_017025123.1	1158	Missense Mutation	CAA,CAC	Q215H	XP_016880612.1
XM_017025124.1	1158	Missense Mutation	CAA,CAC	Q215H	XP_016880613.1
XM_017025125.1	1158	Missense Mutation	CAA,CAC	Q215H	XP_016880614.1
XM_017025126.1	1158	Missense Mutation	CAA,CAC	Q215H	XP_016880615.1
XM_017025127.1	1158	Missense Mutation	CAA,CAC	Q215H	XP_016880616.1
XM_017025128.1	1158	Missense Mutation	AAG,ACG	K185T	XP_016880617.1
XM_017025129.1	1158	Intron			XP_016880618.1
XM_017025130.1	1158	Intron			XP_016880619.1
XM_017025131.1	1158	Intron			XP_016880620.1
XM_017025132.1	1158	Intron			XP_016880621.1
XM_017025133.1	1158	Intron			XP_016880622.1
XM_017025134.1	1158	Intron			XP_016880623.1
XM_017025135.1	1158	Intron			XP_016880624.1
XM_017025136.1	1158	Intron			XP_016880625.1
XM_017025137.1	1158	Intron			XP_016880626.1
XM_017025138.1	1158	Intron			XP_016880627.1
XM_017025139.1	1158	Intron			XP_016880628.1
XM_017025140.1	1158	Intron			XP_016880629.1
XM_017025141.1	1158	Missense Mutation	CAA,CAC	Q215H	XP_016880630.1
XM_017025142.1	1158	Missense Mutation	CAA,CAC	Q215H	XP_016880631.1
XM_017025143.1	1158	Intron			XP_016880632.1
XM_017025144.1	1158	UTR 5			XP_016880633.1

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