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CTGCTCAAGGAGGAGGCCCTGCAGC[A/G]ACATGGAGGGAGCTGCTTTGCTGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603743 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
APOL1 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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APOL1 - apolipoprotein L1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136540.1 | Intron | NP_001130012.1 | ||||
NM_001136541.1 | Intron | NP_001130013.1 | ||||
NM_003661.3 | Intron | NP_003652.2 | ||||
NM_145343.2 | Intron | NP_663318.1 | ||||
XM_005261796.3 | Intron | XP_005261853.1 | ||||
XM_011530478.2 | Intron | XP_011528780.1 |