Research Article
The Association between Genetic Variants and Gene Expression in RAAS Genes Using Captive-Bred Vervet Monkeys (Chlorocebus aethiops)
Table 2
Sequence variants identified in the colony of captive-bred Vervet monkeys (Chlorocebus aethiops).
| Gene | Exon | Nucleotide change | Type of change | AA change | Type of mutation | MutationTaster | PolyPhen-2 | SIFT | VEP |
| AGT | Exon 2 | C195>T | Transition | P65P | Silent | Polymorphism | ND | Neutral | Silent variant | | A228>G | Transition | T76T | Silent | Polymorphism | ND | Neutral | Silent variant | | T266>C | Transition | V89A | Missense | Polymorphism | Benign | Neutral | Missense variant | Exon 3 | C954>A | Transversion | T318T | Silent | Polymorphism | ND | Neutral | Silent variant | Exon 5 | C1431>T | Transition | R477R | Silent | Disease-causing | ND | Neutral | Silent variant |
| CYP3A5 | Exon 5 | G373>C | Transversion | E125Q | SNPs | Polymorphism | PD | Neutral | Missense variant | Exon 10 | G885>T | Transversion | L295L | Silent | Disease-causing | ND | ND | Silent variant | | G888>A | Transition | V296V | Silent | ND | ND | ND | Silent variant |
| GRK4 | Exon 3 | G305>T | Transversion | L102R | SNP | Polymorphism | Benign | Neutral | Missense variant | Exon 5 | C533>T | Transition | A178V | SNP | Polymorphism | Benign | Neutral | Missense variant | Exon 6 | A587>G | Transition | Q196R | SNP | ND | Benign | ND | Missense variant | | G588>C | Transversion | Q196R | SNP | ND | Benign | ND | Missense variant | Exon 11 | G1241>A | Transition | S414N | SNP | Disease-causing | Benign | Deleterious | Missense variant |
| SLC4A5 | Exon 6 | A183>G | Transition | S61S | Silent | Polymorphism | ND | Neutral | Silent variant | Exon 8 | G540>T | Transversion | T180T | Silent | Disease-causing | ND | Neutral | Silent variant | Exon 9 | C705>T | Transition | R235R | Silent | Disease-causing | | Neutral | Silent variant | Exon 17 | G1740>A | Transition | S580S | Silent | Disease-causing | ND | Neutral | Silent variant | Exon 18 | C>1944T | Transition | G648G | Silent | ND | ND | ND | Silent variant | | G1947>C | Transversion | L649F | SNPs | ND | Benign | Neutral | Modifier | Exon 24 | C2817>T | Transition | T939T | Silent | Disease-causing | ND | Neutral | Modifier | Exon 25 | G2892>A | Transition | V964V | Silent | ND | ND | Neutral | ND |
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AA: amino acids; PD: possibly damaging; ND: not determined; SNP: single nucleotide polymorphism; SIFT: Sorting Intolerant from Tolerant; VEP: Variant Effect Predictor.
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