Product Details

SNP ID

rs17006411

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:80132698 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAATCTGCCCAGGTAATCAAGATT[C/T]GACCACTTACAAATTAAATATTCAT

Phenotype

MIM: 614925

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

OTOGL PubMed Links

Additional Information

For this assay, SNP(s) [rs114118181] are located under a primer 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

OTOGL

Gene Name

otogelin like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173591.3		Intron			NP_775862.3
XM_005268802.3		Intron			XP_005268859.1
XM_011538191.1		Intron			XP_011536493.1
XM_011538192.2		Intron			XP_011536494.1
XM_011538193.1		Intron			XP_011536495.1

View Full Product Details