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TCAGCGTCCTGTGTGAGATCAAAGA[C/G]AAAACAGGTAAGACGCTGCGCCCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176312 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC51145 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LOC51145 - uncharacterized LOC51145 | ||||||
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There are no transcripts associated with this gene. |
PBX3 - PBX homeobox 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001134778.1 | 252 | Missense Mutation | GAC,GAG | D,E 14 | NP_001128250.1 | |
NM_006195.5 | 252 | Missense Mutation | GAC,GAG | D,E 89 | NP_006186.1 | |
XM_006717130.1 | 252 | Missense Mutation | GAC,GAG | D,E 89 | XP_006717193.1 | |
XM_006717131.1 | 252 | Missense Mutation | GAC,GAG | D,E 89 | XP_006717194.1 | |
XM_006717132.1 | 252 | Missense Mutation | GAC,GAG | D,E 89 | XP_006717195.1 | |
XM_006717133.1 | 252 | UTR 5 | XP_006717196.1 | |||
XM_011518755.1 | 252 | Missense Mutation | GAC,GAG | D,E 14 | XP_011517057.1 | |
XM_017014786.1 | 252 | Missense Mutation | GAC,GAG | D,E 14 | XP_016870275.1 |