Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35530 | A02 | 30526525 | C | T | synonymous_variant | LOW | c.255C>T|p.Ala85Ala |
S179 |
2 | BAA02g35530 | A02 | 30526729 | G | A | synonymous_variant | LOW | c.459G>A|p.Lys153Lys |
S122 |
3 | BAA02g35530 | A02 | 30526979 | G | A | synonymous_variant | LOW | c.600G>A|p.Arg200Arg |
S56 |
4 | BAA02g35530 | A02 | 30527153 | C | T | intron_variant | MODIFIER | c.765+9C>T| |
S221 |
5 | BAA02g35530 | A02 | 30528895 | C | T | synonymous_variant | LOW | c.1593C>T|p.Ala531Ala |
S87 |
6 | BAA02g35530 | A02 | 30530263 | G | A | missense_variant | MODERATE | c.2191G>A|p.Gly731Arg |
S11 |
7 | BAA02g35530 | A02 | 30530286 | C | T | synonymous_variant | LOW | c.2214C>T|p.Thr738Thr |
S121 |
8 | BAA02g35530 | A02 | 30530485 | G | A | synonymous_variant | LOW | c.2301G>A|p.Glu767Glu |
S113 |
9 | BAA02g35530 | A02 | 30531808 | C | T | missense_variant | MODERATE | c.2978C>T|p.Pro993Leu |
S136 S40 S49 |
10 | BAA02g35530 | A02 | 30532821 | C | T | missense_variant | MODERATE | c.3448C>T|p.Leu1150Phe |
S88 |
11 | BAA02g35530 | A02 | 30533172 | C | T | synonymous_variant | LOW | c.3579C>T|p.Tyr1193Tyr |
S233 |
12 | BAA02g35530 | A02 | 30536362 | G | A | downstream_gene_variant | MODIFIER | c.*3103G>A| |
S268 |
13 | BAA02g35530 | A02 | 30537620 | G | A | downstream_gene_variant | MODIFIER | c.*4361G>A| |
S279 |