| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g41450 | A03 | 19431967 | C | T | upstream_gene_variant | MODIFIER | c.-3699C>T| |
S301 S304 |
| 2 | BAA03g41450 | A03 | 19434347 | C | T | upstream_gene_variant | MODIFIER | c.-1319C>T| |
S16 |
| 3 | BAA03g41450 | A03 | 19435103 | G | A | upstream_gene_variant | MODIFIER | c.-563G>A| |
S265 |
| 4 | BAA03g41450 | A03 | 19435321 | C | T | upstream_gene_variant | MODIFIER | c.-345C>T| |
S188 S276 S298 |
| 5 | BAA03g41450 | A03 | 19435716 | G | A | synonymous_variant | LOW | c.51G>A|p.Arg17Arg |
S223 |
| 6 | BAA03g41450 | A03 | 19436362 | C | T | missense_variant | MODERATE | c.697C>T|p.Pro233Ser |
S105 S106 |
| 7 | BAA03g41450 | A03 | 19436633 | C | T | missense_variant | MODERATE | c.968C>T|p.Ala323Val |
S73 S91 |
| 8 | BAA03g41450 | A03 | 19436642 | C | T | missense_variant | MODERATE | c.977C>T|p.Ala326Val |
S163 |
| 9 | BAA03g41450 | A03 | 19436903 | C | T | missense_variant | MODERATE | c.1154C>T|p.Thr385Ile |
S105 S106 |
| 10 | BAA03g41450 | A03 | 19437116 | C | T | missense_variant | MODERATE | c.1367C>T|p.Pro456Leu |
S156 |
| 11 | BAA03g41450 | A03 | 19437910 | G | A | splice_region_variant&intron_variant | LOW | c.1786+7G>A| |
S296 |
| 12 | BAA03g41450 | A03 | 19438090 | C | T | synonymous_variant | LOW | c.1896C>T|p.Pro632Pro |
S190 |
| 13 | BAA03g41450 | A03 | 19439592 | G | A | downstream_gene_variant | MODIFIER | c.*639G>A| |
S306 S308 |
| 14 | BAA03g41450 | A03 | 19440211 | G | A | downstream_gene_variant | MODIFIER | c.*1258G>A| |
S132 S215 S89 |