Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19850 | A02 | 10426581 | C | T | upstream_gene_variant | MODIFIER | c.-3052C>T| |
S167 |
2 | BAA02g19850 | A02 | 10427352 | G | A | upstream_gene_variant | MODIFIER | c.-2281G>A| |
S206 S26 |
3 | BAA02g19850 | A02 | 10429925 | G | A | missense_variant | MODERATE | c.220G>A|p.Ala74Thr |
S134 |
4 | BAA02g19850 | A02 | 10430385 | C | T | synonymous_variant | LOW | c.471C>T|p.Ile157Ile |
S77 S82 |
5 | BAA02g19850 | A02 | 10430386 | C | T | stop_gained | HIGH | c.472C>T|p.Arg158* |
S183 S198 |
6 | BAA02g19850 | A02 | 10431108 | C | T | missense_variant | MODERATE | c.865C>T|p.His289Tyr |
S73 |
7 | BAA02g19850 | A02 | 10432249 | C | T | intron_variant | MODIFIER | c.882-251C>T| |
S255 |
8 | BAA02g19850 | A02 | 10432414 | C | T | intron_variant | MODIFIER | c.882-86C>T| |
S250 |
9 | BAA02g19850 | A02 | 10432834 | C | T | missense_variant | MODERATE | c.1216C>T|p.Leu406Phe |
S219 S72 |
10 | BAA02g19850 | A02 | 10434662 | C | T | downstream_gene_variant | MODIFIER | c.*1253C>T| |
S105 S106 |