Product Details

SNP ID
rs150874436
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:125747615 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGGCGACATCCTCCACCAGATCAT[A/G]ACCATCACCGACCAGAGCTTGGACG
Phenotype
MIM: 176312
Polymorphism
A/G, Transition 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_001134778.1 147 Intron NP_001128250.1
NM_006195.5 147 Missense Mutation ATA,ATG I54M NP_006186.1
XM_006717130.1 147 Missense Mutation ATA,ATG I54M XP_006717193.1
XM_006717131.1 147 Missense Mutation ATA,ATG I54M XP_006717194.1
XM_006717132.1 147 Missense Mutation ATA,ATG I54M XP_006717195.1
XM_006717133.1 147 UTR 5 XP_006717196.1
XM_011518755.1 147 Intron XP_011517057.1
XM_017014786.1 147 Intron XP_016870275.1

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