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CCACAGGGGAAAGGGGGGACTTTCC[A/G]GGAACTTACGTAGAATATATTGGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 171833 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PIK3R1 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 - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PIK3R1 - phosphoinositide-3-kinase regulatory subunit 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242466.1 | 1582 | Intron | NP_001229395.1 | |||
NM_181504.3 | 1582 | Intron | NP_852556.2 | |||
NM_181523.2 | 1582 | Silent Mutation | CCA,CCG | P,P 70 | NP_852664.1 | |
NM_181524.1 | 1582 | Intron | NP_852665.1 | |||
XM_005248542.3 | 1582 | Silent Mutation | CCA,CCG | P,P 70 | XP_005248599.1 | |
XM_011543493.2 | 1582 | Intron | XP_011541795.1 | |||
XM_017009585.1 | 1582 | Silent Mutation | CCA,CCG | P,P 70 | XP_016865074.1 | |
XM_017009586.1 | 1582 | Intron | XP_016865075.1 |