Product Details

SNP ID

rs149325199

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:36678950 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGATGGATTAAAGGGTTAACTTTT[A/C]AAGATTATTATTGGTTAATGTTGAC

Phenotype

MIM: 167416 MIM: 607571

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

PAX9 PubMed Links

Additional Information

For this assay, SNP(s) [rs5807898] 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

PAX9

Gene Name

paired box 9

There are no transcripts associated with this gene.

Gene

SLC25A21

Gene Name

solute carrier family 25 member 21

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001171170.1	2918	Intron			NP_001164641.1
NM_030631.3	2918	UTR 3			NP_085134.1
XM_011537287.2	2918	Intron			XP_011535589.1
XM_011537288.2	2918	Intron			XP_011535590.1
XM_011537289.2	2918	Intron			XP_011535591.1

View Full Product Details