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TCGGCGACATCCTCCACCAGATCAT[A/G]ACCATCACCGACCAGAGCTTGGACG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 147 | Intron | NP_001128250.1 | |||
NM_006195.5 | 147 | Missense Mutation | ATA,ATG | I,M 54 | NP_006186.1 | |
XM_006717130.1 | 147 | Missense Mutation | ATA,ATG | I,M 54 | XP_006717193.1 | |
XM_006717131.1 | 147 | Missense Mutation | ATA,ATG | I,M 54 | XP_006717194.1 | |
XM_006717132.1 | 147 | Missense Mutation | ATA,ATG | I,M 54 | 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 |