| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g01230 | A08 | 874453 | C | T | missense_variant | MODERATE | c.1139G>A|p.Cys380Tyr |
S105 S106 |
| 2 | BAA08g01230 | A08 | 881913 | C | T | intron_variant | MODIFIER | c.280-2218G>A| |
S153 S213 |
| 3 | BAA08g01230 | A08 | 882555 | C | T | intron_variant | MODIFIER | c.280-2860G>A| |
S70 |
| 4 | BAA08g01230 | A08 | 884870 | C | T | intron_variant | MODIFIER | c.280-5175G>A| |
S294 |
| 5 | BAA08g01230 | A08 | 885638 | C | T | intron_variant | MODIFIER | c.280-5943G>A| |
S245 |
| 6 | BAA08g01230 | A08 | 886615 | C | T | intron_variant | MODIFIER | c.280-6920G>A| |
S163 |
| 7 | BAA08g01230 | A08 | 886721 | C | A | intron_variant | MODIFIER | c.280-7026G>T| |
S262 |
| 8 | BAA08g01230 | A08 | 886991 | G | A | intron_variant | MODIFIER | c.280-7296C>T| |
S32 |
| 9 | BAA08g01230 | A08 | 887657 | C | T | intron_variant | MODIFIER | c.279+7561G>A| |
S175 |
| 10 | BAA08g01230 | A08 | 891717 | C | T | intron_variant | MODIFIER | c.279+3501G>A| |
S305 |
| 11 | BAA08g01230 | A08 | 892428 | C | T | intron_variant | MODIFIER | c.279+2790G>A| |
S89 |
| 12 | BAA08g01230 | A08 | 892492 | G | A | intron_variant | MODIFIER | c.279+2726C>T| |
S217 |
| 13 | BAA08g01230 | A08 | 892662 | G | A | intron_variant | MODIFIER | c.279+2556C>T| |
S20 |
| 14 | BAA08g01230 | A08 | 898362 | C | T | missense_variant | MODERATE | c.20G>A|p.Gly7Glu |
S203 |
| 15 | BAA08g01230 | A08 | 899131 | G | A | upstream_gene_variant | MODIFIER | c.-750C>T| |
S95 |
| 16 | BAA08g01230 | A08 | 899223 | C | T | upstream_gene_variant | MODIFIER | c.-842G>A| |
S201 |
| 17 | BAA08g01230 | A08 | 901423 | C | T | upstream_gene_variant | MODIFIER | c.-3042G>A| |
S163 |
| 18 | BAA08g01230 | A08 | 902153 | C | T | upstream_gene_variant | MODIFIER | c.-3772G>A| |
S80 |