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APOL3TGCAAGGAAGATGCCTGAAGTGGTC[A/G]CACTCAGGATCCGGGCTCCTCTGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
APOL3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| APOL3 - apolipoprotein L3 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_014349.2 | 1996 | Missense Mutation | GAG,GGG | E,G 271 | NP_055164.1 | |
| NM_030644.1 | 1996 | Missense Mutation | GAG,GGG | E,G 271 | NP_085147.1 | |
| NM_145639.1 | 1996 | Missense Mutation | GAG,GGG | E,G 271 | NP_663614.1 | |
| NM_145640.2 | 1996 | Missense Mutation | GAG,GGG | E,G 342 | NP_663615.1 | |
| NM_145641.2 | 1996 | Missense Mutation | GAG,GGG | E,G 142 | NP_663616.1 | |
| NM_145642.2 | 1996 | Missense Mutation | GAG,GGG | E,G 142 | NP_663617.1 | |
| XM_006724324.1 | 1996 | Missense Mutation | XP_006724387.1 | |||
| XM_006724325.2 | 1996 | Missense Mutation | XP_006724388.1 | |||
| XM_017028946.1 | 1996 | Missense Mutation | XP_016884435.1 | |||
| XM_017028947.1 | 1996 | Missense Mutation | XP_016884436.1 | |||
| XM_017028948.1 | 1996 | Missense Mutation | XP_016884437.1 | |||
| XM_017028949.1 | 1996 | Missense Mutation | XP_016884438.1 | |||
| XM_017028950.1 | 1996 | Missense Mutation | XP_016884439.1 | |||
| XM_017028951.1 | 1996 | Missense Mutation | XP_016884440.1 | |||
| XM_017028952.1 | 1996 | Missense Mutation | XP_016884441.1 | |||