Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAACTTCCCCATGTTCTTTTTATAC[C/T]GGATTCTTTTGTTGCCAAACCAGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608127 | ||||||||||||||||||||
Literature Links: |
PBX4 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 |
PBX4 - PBX homeobox 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_025245.2 | 768 | Missense Mutation | CAG,CGG | Q,R 267 | NP_079521.1 | |
XM_006722911.3 | 768 | Missense Mutation | CAG,CGG | Q,R 181 | XP_006722974.1 | |
XM_011528320.2 | 768 | Missense Mutation | CAG,CGG | Q,R 284 | XP_011526622.1 | |
XM_011528322.2 | 768 | Missense Mutation | CAG,CGG | Q,R 181 | XP_011526624.1 | |
XM_017027326.1 | 768 | Missense Mutation | CAG,CGG | Q,R 250 | XP_016882815.1 | |
XM_017027327.1 | 768 | Missense Mutation | CAG,CGG | Q,R 236 | XP_016882816.1 | |
XM_017027328.1 | 768 | Missense Mutation | CAG,CGG | Q,R 284 | XP_016882817.1 | |
XM_017027329.1 | 768 | Missense Mutation | CAG,CGG | Q,R 102 | XP_016882818.1 | |
XM_017027330.1 | 768 | Intron | XP_016882819.1 |