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TAGGACATGAAGGTCTTCATTAAGG[A/C]AACATAATAAACTGTGTAGCCTCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
11 submissions
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Phenotype: |
MIM: 176310 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PBX1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
PBX1 - PBX homeobox 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204961.1 | Intron | NP_001191890.1 | ||||
NM_001204963.1 | Intron | NP_001191892.1 | ||||
NM_002585.3 | Intron | NP_002576.1 | ||||
XM_005245228.3 | Intron | XP_005245285.1 | ||||
XM_005245229.3 | Intron | XP_005245286.1 | ||||
XM_011509590.1 | Intron | XP_011507892.1 | ||||
XM_011509591.2 | Intron | XP_011507893.1 | ||||
XM_011509592.1 | Intron | XP_011507894.1 | ||||
XM_017001395.1 | Intron | XP_016856884.1 | ||||
XM_017001396.1 | Intron | XP_016856885.1 |