Product Details

SNP ID

rs17104888

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:36660959 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTGCAGCGTCGGTGTCCACTGTCT[C/T]GGGACTAAGTCTCTTTCATATTTAA

Phenotype

MIM: 167416

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PAX9 PubMed Links

Gene Details

Gene

PAX9

Gene Name

paired box 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006194.3		Intron			NP_006185.1

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