Product Details

SNP ID
rs199866010
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:125748616 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAGCGTCCTGTGTGAGATCAAAGA[C/G]AAAACAGGTAAGACGCTGCGCCCCG
Phenotype
MIM: 176312
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
LOC51145 PubMed Links

Gene Details

Gene
LOC51145
Gene Name
uncharacterized LOC51145
There are no transcripts associated with this gene.

Gene
PBX3
Gene Name
PBX homeobox 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001134778.1 252 Missense Mutation GAC,GAG D14E NP_001128250.1
NM_006195.5 252 Missense Mutation GAC,GAG D89E NP_006186.1
XM_006717130.1 252 Missense Mutation GAC,GAG D89E XP_006717193.1
XM_006717131.1 252 Missense Mutation GAC,GAG D89E XP_006717194.1
XM_006717132.1 252 Missense Mutation GAC,GAG D89E XP_006717195.1
XM_006717133.1 252 UTR 5 XP_006717196.1
XM_011518755.1 252 Missense Mutation GAC,GAG D14E XP_011517057.1
XM_017014786.1 252 Missense Mutation GAC,GAG D14E XP_016870275.1

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