Product Details

SNP ID

rs78313274

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:50726320 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTTACCATCATCCCCCTGATATAA[A/C]GCAAAATTCTGAAAACCCATAATTT

Phenotype

MIM: 608684

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

NIN PubMed Links

Additional Information

For this assay, SNP(s) [rs369910232] 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

NIN

Gene Name

ninein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016350.4		Intron			NP_057434.4
NM_020921.3		Intron			NP_065972.3
NM_182944.2		Intron			NP_891989.2
NM_182946.1		Intron			NP_891991.1
XM_011536817.1		Intron			XP_011535119.1
XM_011536819.2		Intron			XP_011535121.1
XM_011536822.1		Intron			XP_011535124.1
XM_011536823.2		Intron			XP_011535125.1

View Full Product Details