Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35540 | A02 | 30531669 | C | T | upstream_gene_variant | MODIFIER | c.-4390C>T| |
S32 |
2 | BAA02g35540 | A02 | 30532382 | G | A | upstream_gene_variant | MODIFIER | c.-3677G>A| |
S67 |
3 | BAA02g35540 | A02 | 30532451 | G | A | upstream_gene_variant | MODIFIER | c.-3608G>A| |
S61 |
4 | BAA02g35540 | A02 | 30532550 | C | T | upstream_gene_variant | MODIFIER | c.-3509C>T| |
S308 |
5 | BAA02g35540 | A02 | 30534367 | C | T | upstream_gene_variant | MODIFIER | c.-1692C>T| |
S17 S62 |
6 | BAA02g35540 | A02 | 30534438 | G | A | upstream_gene_variant | MODIFIER | c.-1621G>A| |
S166 |
7 | BAA02g35540 | A02 | 30534537 | G | A | upstream_gene_variant | MODIFIER | c.-1522G>A| |
S153 S213 |
8 | BAA02g35540 | A02 | 30536089 | C | T | stop_gained | HIGH | c.31C>T|p.Arg11* |
S241 |
9 | BAA02g35540 | A02 | 30536236 | C | T | missense_variant | MODERATE | c.178C>T|p.Pro60Ser |
S296 |
10 | BAA02g35540 | A02 | 30537182 | C | T | missense_variant | MODERATE | c.428C>T|p.Ala143Val |
S195 |
11 | BAA02g35540 | A02 | 30537211 | C | T | missense_variant | MODERATE | c.457C>T|p.Leu153Phe |
S124 |
12 | BAA02g35540 | A02 | 30537238 | C | T | stop_gained | HIGH | c.484C>T|p.Gln162* |
S218 |
13 | BAA02g35540 | A02 | 30539469 | C | T | downstream_gene_variant | MODIFIER | c.*2112C>T| |
S83 |
14 | BAA02g35540 | A02 | 30540944 | C | T | downstream_gene_variant | MODIFIER | c.*3587C>T| |
S179 |