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GTAAGTTGGGTGTGATGTCACGCAT[A/G]ACTTCCTTAAATACCTTCAATCGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607253 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
APOL3 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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APOL3 - apolipoprotein L3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014349.2 | 1778 | Silent Mutation | GTC,GTT | V,V 198 | NP_055164.1 | |
NM_030644.1 | 1778 | Silent Mutation | GTC,GTT | V,V 198 | NP_085147.1 | |
NM_145639.1 | 1778 | Silent Mutation | GTC,GTT | V,V 198 | NP_663614.1 | |
NM_145640.2 | 1778 | Silent Mutation | GTC,GTT | V,V 269 | NP_663615.1 | |
NM_145641.2 | 1778 | Silent Mutation | GTC,GTT | V,V 69 | NP_663616.1 | |
NM_145642.2 | 1778 | Silent Mutation | GTC,GTT | V,V 69 | NP_663617.1 | |
XM_006724324.1 | 1778 | Silent Mutation | GTC,GTT | V,V 198 | XP_006724387.1 | |
XM_006724325.2 | 1778 | Silent Mutation | GTC,GTT | V,V 198 | XP_006724388.1 | |
XM_017028946.1 | 1778 | Silent Mutation | GTC,GTT | V,V 199 | XP_016884435.1 | |
XM_017028947.1 | 1778 | Silent Mutation | GTC,GTT | V,V 199 | XP_016884436.1 | |
XM_017028948.1 | 1778 | Silent Mutation | GTC,GTT | V,V 199 | XP_016884437.1 | |
XM_017028949.1 | 1778 | Silent Mutation | GTC,GTT | V,V 199 | XP_016884438.1 | |
XM_017028950.1 | 1778 | Silent Mutation | GTC,GTT | V,V 199 | XP_016884439.1 | |
XM_017028951.1 | 1778 | Silent Mutation | GTC,GTT | V,V 199 | XP_016884440.1 | |
XM_017028952.1 | 1778 | Silent Mutation | GTC,GTT | V,V 69 | XP_016884441.1 |