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TTACATGAAGCACGCCACCAAGACC[A/G]CCAAGGATGCACTGAGCAGCGTGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 107680 MIM: 107690 MIM: 107720 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
APOA1 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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APOA1 - apolipoprotein A1 | ||||||
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There are no transcripts associated with this gene. |
APOA1-AS - APOA1 antisense RNA | ||||||
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There are no transcripts associated with this gene. |
APOA4 - apolipoprotein A4 | ||||||
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There are no transcripts associated with this gene. |
APOC3 - apolipoprotein C3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000040.1 | 173 | Missense Mutation | ACC,GCC | T,A 43 | NP_000031.1 |