Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCTGCAGGCCTCTGCAATGTCACC[A/G]CCTCTGTGTCCCCTCCTTCTCCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
49 submissions
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Phenotype: |
MIM: 610278 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
PEAR1 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
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CEPH (CEU)
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EAS
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African American
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YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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PEAR1 - platelet endothelial aggregation receptor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080471.1 | 1328 | Silent Mutation | CCA,CCG | P,P 3 | NP_001073940.1 | |
XM_005245141.3 | 1328 | Silent Mutation | CCA,CCG | P,P 3 | XP_005245198.1 | |
XM_011509510.2 | 1328 | Silent Mutation | CCA,CCG | P,P 3 | XP_011507812.1 | |
XM_011509511.2 | 1328 | Silent Mutation | CCA,CCG | P,P 3 | XP_011507813.1 | |
XM_011509512.2 | 1328 | UTR 5 | XP_011507814.1 | |||
XM_017001234.1 | 1328 | Missense Mutation | CAC,CGC | H,R 73 | XP_016856723.1 | |
XM_017001235.1 | 1328 | Missense Mutation | CAC,CGC | H,R 73 | XP_016856724.1 | |
XM_017001236.1 | 1328 | Silent Mutation | CCA,CCG | P,P 3 | XP_016856725.1 | |
XM_017001237.1 | 1328 | UTR 5 | XP_016856726.1 | |||
XM_017001238.1 | 1328 | UTR 5 | XP_016856727.1 | |||
XM_017001239.1 | 1328 | UTR 5 | XP_016856728.1 | |||
XM_017001240.1 | 1328 | Intron | XP_016856729.1 | |||
XM_017001241.1 | 1328 | Intron | XP_016856730.1 | |||
XM_017001242.1 | 1328 | Intron | XP_016856731.1 |
Set Membership: |
HapMap Validated |