Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g68440 | A09 | 61548413 | C | T | upstream_gene_variant | MODIFIER | c.-4577C>T| |
S172 S217 |
2 | BAA09g68440 | A09 | 61553098 | G | A | missense_variant | MODERATE | c.109G>A|p.Gly37Ser |
S225 S73 |
3 | BAA09g68440 | A09 | 61553141 | C | T | missense_variant | MODERATE | c.152C>T|p.Ala51Val |
S117 |
4 | BAA09g68440 | A09 | 61553165 | C | T | missense_variant | MODERATE | c.176C>T|p.Ser59Leu |
S157 S163 |
5 | BAA09g68440 | A09 | 61553642 | C | T | synonymous_variant | LOW | c.267C>T|p.Cys89Cys |
S18 |
6 | BAA09g68440 | A09 | 61553718 | C | T | missense_variant | MODERATE | c.343C>T|p.Leu115Phe |
S157 S163 |
7 | BAA09g68440 | A09 | 61553731 | C | T | missense_variant | MODERATE | c.356C>T|p.Thr119Met |
S97 |
8 | BAA09g68440 | A09 | 61554882 | C | T | missense_variant | MODERATE | c.887C>T|p.Ala296Val |
S138 |
9 | BAA09g68440 | A09 | 61554895 | G | A | synonymous_variant | LOW | c.900G>A|p.Lys300Lys |
S177 |
10 | BAA09g68440 | A09 | 61556941 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1655-1G>A| |
S263 |