Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g06200 | A04 | 4049639 | G | A | missense_variant | MODERATE | c.139G>A|p.Ala47Thr |
S256 |
2 | BAA04g06200 | A04 | 4049698 | G | A | synonymous_variant | LOW | c.198G>A|p.Ala66Ala |
S108 |
3 | BAA04g06200 | A04 | 4049823 | C | T | missense_variant | MODERATE | c.323C>T|p.Thr108Ile |
S68 |
4 | BAA04g06200 | A04 | 4050115 | G | A | stop_gained | HIGH | c.615G>A|p.Trp205* |
S245 |
5 | BAA04g06200 | A04 | 4050194 | C | T | missense_variant | MODERATE | c.694C>T|p.Arg232Cys |
S200 |
6 | BAA04g06200 | A04 | 4050404 | G | A | missense_variant | MODERATE | c.904G>A|p.Ala302Thr |
S67 |
7 | BAA04g06200 | A04 | 4050659 | G | A | missense_variant | MODERATE | c.1159G>A|p.Glu387Lys |
S40 S49 |
8 | BAA04g06200 | A04 | 4051247 | G | A | missense_variant | MODERATE | c.1747G>A|p.Gly583Ser |
S269 |
9 | BAA04g06200 | A04 | 4052372 | G | A | missense_variant | MODERATE | c.2872G>A|p.Gly958Ser |
S153 S213 |
10 | BAA04g06200 | A04 | 4059052 | C | T | downstream_gene_variant | MODIFIER | c.*4848C>T| |
S308 |