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CCTGGGAGATGGTGAGGCCGCCCTT[C/T]CTGGCCAGCTCTTCTTTGGCTTCTT
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 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_025245.2 | 712 | Silent Mutation | AGA,AGG | R,R 248 | NP_079521.1 | |
XM_006722911.3 | 712 | Silent Mutation | AGA,AGG | R,R 162 | XP_006722974.1 | |
XM_011528320.2 | 712 | Silent Mutation | AGA,AGG | R,R 265 | XP_011526622.1 | |
XM_011528322.2 | 712 | Silent Mutation | AGA,AGG | R,R 162 | XP_011526624.1 | |
XM_017027326.1 | 712 | Silent Mutation | AGA,AGG | R,R 231 | XP_016882815.1 | |
XM_017027327.1 | 712 | Silent Mutation | AGA,AGG | R,R 217 | XP_016882816.1 | |
XM_017027328.1 | 712 | Silent Mutation | AGA,AGG | R,R 265 | XP_016882817.1 | |
XM_017027329.1 | 712 | Silent Mutation | AGA,AGG | R,R 83 | XP_016882818.1 | |
XM_017027330.1 | 712 | Intron | XP_016882819.1 |