| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g00720 | A07 | 452188 | C | T | missense_variant | MODERATE | c.1417G>A|p.Val473Ile |
S104 S52 |
| 2 | BAA07g00720 | A07 | 453164 | G | A | missense_variant | MODERATE | c.677C>T|p.Ala226Val |
S188 |
| 3 | BAA07g00720 | A07 | 453167 | G | A | missense_variant | MODERATE | c.674C>T|p.Ala225Val |
S98 |
| 4 | BAA07g00720 | A07 | 453783 | G | A | missense_variant | MODERATE | c.205C>T|p.Pro69Ser |
S182 |
| 5 | BAA07g00720 | A07 | 453994 | G | A | stop_gained | HIGH | c.79C>T|p.Gln27* |
S262 |
| 6 | BAA07g00720 | A07 | 454204 | C | T | upstream_gene_variant | MODIFIER | c.-132G>A| |
S34 |
| 7 | BAA07g00720 | A07 | 454372 | G | A | upstream_gene_variant | MODIFIER | c.-300C>T| |
S278 |
| 8 | BAA07g00720 | A07 | 454389 | G | A | upstream_gene_variant | MODIFIER | c.-317C>T| |
S239 |
| 9 | BAA07g00720 | A07 | 454456 | G | A | upstream_gene_variant | MODIFIER | c.-384C>T| |
S190 |
| 10 | BAA07g00720 | A07 | 457562 | C | T | upstream_gene_variant | MODIFIER | c.-3490G>A| |
S82 S92 |
| 11 | BAA07g00720 | A07 | 457813 | C | T | upstream_gene_variant | MODIFIER | c.-3741G>A| |
S230 |
| 12 | BAA07g00720 | A07 | 458092 | T | A | upstream_gene_variant | MODIFIER | c.-4020A>T| |
S146 |
| 13 | BAA07g00720 | A07 | 458963 | G | A | upstream_gene_variant | MODIFIER | c.-4891C>T| |
S266 |