Product Details

SNP ID

rs12449676

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:75591829 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCTTTCAGCCAGGAGAGGGGTGGT[C/T]TCCAGGCCTCTGGCGTCTCCTGGGG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MYO15B PubMed Links

Additional Information

For this assay, SNP(s) [rs114737951] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

MYO15B

Gene Name

myosin XVB

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001309242.1		Intron			NP_001296171.1
XM_017025120.1		Intron			XP_016880609.1
XM_017025121.1		Intron			XP_016880610.1
XM_017025122.1		Intron			XP_016880611.1
XM_017025123.1		Intron			XP_016880612.1
XM_017025124.1		Intron			XP_016880613.1
XM_017025125.1		Intron			XP_016880614.1
XM_017025126.1		Intron			XP_016880615.1
XM_017025127.1		Intron			XP_016880616.1
XM_017025128.1		Intron			XP_016880617.1
XM_017025129.1		Intron			XP_016880618.1
XM_017025130.1		Intron			XP_016880619.1
XM_017025131.1		Intron			XP_016880620.1
XM_017025132.1		Intron			XP_016880621.1
XM_017025133.1		Intron			XP_016880622.1
XM_017025134.1		Intron			XP_016880623.1
XM_017025135.1		Intron			XP_016880624.1
XM_017025136.1		Intron			XP_016880625.1
XM_017025137.1		Intron			XP_016880626.1
XM_017025138.1		Intron			XP_016880627.1
XM_017025139.1		Intron			XP_016880628.1
XM_017025140.1		Intron			XP_016880629.1
XM_017025141.1		Intron			XP_016880630.1
XM_017025142.1		Intron			XP_016880631.1
XM_017025143.1		Intron			XP_016880632.1
XM_017025144.1		Intron			XP_016880633.1

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