Product Details

SNP ID

rs17081968

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:70016696 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCCTCCATCTGTCCTACATCTCAGA[G/T]AATGAAGTCTCTGCGAGGCTCACTG

Phenotype

MIM: 610436

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

RTTN PubMed Links

Additional Information

For this assay, SNP(s) [rs116199131] 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

RTTN

Gene Name

rotatin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318520.1		Intron			NP_001305449.1
NM_173630.3		Intron			NP_775901.3
XM_006722434.3		Intron			XP_006722497.1
XM_006722435.3		Intron			XP_006722498.1
XM_011525902.2		Intron			XP_011524204.1
XM_011525903.2		Intron			XP_011524205.1
XM_011525904.2		Intron			XP_011524206.1
XM_011525905.2		Intron			XP_011524207.1
XM_011525906.2		Intron			XP_011524208.1
XM_011525907.2		Intron			XP_011524209.1
XM_011525908.2		Intron			XP_011524210.1
XM_017025693.1		Intron			XP_016881182.1
XM_017025694.1		Intron			XP_016881183.1
XM_017025695.1		Intron			XP_016881184.1
XM_017025696.1		Intron			XP_016881185.1

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