Product Details

SNP ID
hCV27834583
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:36659231 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGTGTAACCAGGCGGCAGACTCC[A/G]GCTGACCCTTGTTCTTGTTCTAGGT
Phenotype
MIM: 167416
Polymorphism
A/G, 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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