Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g02000 | A05 | 1086603 | C | T | missense_variant | MODERATE | c.1062G>A|p.Met354Ile |
S197 |
2 | BAA05g02000 | A05 | 1087248 | C | T | missense_variant | MODERATE | c.625G>A|p.Ala209Thr |
S189 |
3 | BAA05g02000 | A05 | 1087758 | C | T | synonymous_variant | LOW | c.375G>A|p.Glu125Glu |
S136 |
4 | BAA05g02000 | A05 | 1087984 | G | A | missense_variant | MODERATE | c.301C>T|p.Pro101Ser |
S5 |
5 | BAA05g02000 | A05 | 1088443 | G | A | missense_variant | MODERATE | c.41C>T|p.Ala14Val |
S186 |
6 | BAA05g02000 | A05 | 1088661 | G | A | upstream_gene_variant | MODIFIER | c.-178C>T| |
S245 |
7 | BAA05g02000 | A05 | 1089428 | G | A | upstream_gene_variant | MODIFIER | c.-945C>T| |
S200 |
8 | BAA05g02000 | A05 | 1090729 | C | T | upstream_gene_variant | MODIFIER | c.-2246G>A| |
S270 |
9 | BAA05g02000 | A05 | 1092663 | G | T | upstream_gene_variant | MODIFIER | c.-4180C>A| |
S56 |