Product Details

SNP ID
rs12033962
Assay Type
Functionally tested
NCBI dbSNP Submissions
23
Location
Chr.1:164559633 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCACGCCCCCTCCCCCTCCCCCTCC[C/T]CATCCTCCCACCATCCTCTAAAGAG
Phenotype
MIM: 176310
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PBX1 PubMed Links

Gene Details

Gene
PBX1
Gene Name
PBX homeobox 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001204961.1 274 UTR 5 NP_001191890.1
NM_001204963.1 274 UTR 5 NP_001191892.1
NM_002585.3 274 UTR 5 NP_002576.1
XM_005245228.3 274 UTR 5 XP_005245285.1
XM_005245229.3 274 Intron XP_005245286.1
XM_011509590.1 274 UTR 5 XP_011507892.1
XM_011509591.2 274 UTR 5 XP_011507893.1
XM_011509592.1 274 UTR 5 XP_011507894.1
XM_017001395.1 274 UTR 5 XP_016856884.1
XM_017001396.1 274 UTR 5 XP_016856885.1

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