Product Details

SNP ID
rs141026836
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:36678215 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCTTCGTTTAAAACTCAGATGGC[C/T]AGATTAGTTAGGTTTTCAAATCACT
Phenotype
MIM: 167416 MIM: 607571
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 1476 Intron NP_006185.1
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 1476 UTR 3 NP_001164641.1
NM_030631.3 1476 UTR 3 NP_085134.1
XM_011537287.2 1476 Intron XP_011535589.1
XM_011537288.2 1476 Intron XP_011535590.1
XM_011537289.2 1476 Intron XP_011535591.1

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