Product Details

SNP ID: rs17104892
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.14:36662394 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AGCAAACCAAGTTTTGTTTCACACG[C/G]GCGCACACATGCAAACAAAACAGGA
Phenotype: MIM: 167416
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: PAX9 PubMed Links

Gene Details

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