| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g15860 | A07 | 22913005 | C | T | upstream_gene_variant | MODIFIER | c.-4451C>T| |
S1 S90 |
| 2 | BAA07g15860 | A07 | 22914092 | G | A | upstream_gene_variant | MODIFIER | c.-3364G>A| |
S188 |
| 3 | BAA07g15860 | A07 | 22916076 | G | A | upstream_gene_variant | MODIFIER | c.-1380G>A| |
S44 |
| 4 | BAA07g15860 | A07 | 22916098 | G | A | upstream_gene_variant | MODIFIER | c.-1358G>A| |
S131 |
| 5 | BAA07g15860 | A07 | 22916527 | G | A | upstream_gene_variant | MODIFIER | c.-929G>A| |
S255 |
| 6 | BAA07g15860 | A07 | 22916799 | C | T | upstream_gene_variant | MODIFIER | c.-657C>T| |
S277 |
| 7 | BAA07g15860 | A07 | 22918340 | C | T | missense_variant | MODERATE | c.734C>T|p.Pro245Leu |
S157 S265 |
| 8 | BAA07g15860 | A07 | 22918541 | C | T | missense_variant | MODERATE | c.935C>T|p.Pro312Leu |
S4 |
| 9 | BAA07g15860 | A07 | 22920300 | G | A | missense_variant | MODERATE | c.1744G>A|p.Gly582Arg |
S184 |
| 10 | BAA07g15860 | A07 | 22921224 | G | A | missense_variant | MODERATE | c.2329G>A|p.Ala777Thr |
S2 |
| 11 | BAA07g15860 | A07 | 22921334 | G | A | stop_gained | HIGH | c.2439G>A|p.Trp813* |
S47 S74 |