| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g12380 | A08 | 10815149 | C | T | upstream_gene_variant | MODIFIER | c.-4951C>T| |
S46 |
| 2 | BAA08g12380 | A08 | 10815958 | G | A | upstream_gene_variant | MODIFIER | c.-4142G>A| |
S298 |
| 3 | BAA08g12380 | A08 | 10816071 | C | T | upstream_gene_variant | MODIFIER | c.-4029C>T| |
S168 |
| 4 | BAA08g12380 | A08 | 10816189 | G | A | upstream_gene_variant | MODIFIER | c.-3911G>A| |
S11 |
| 5 | BAA08g12380 | A08 | 10820291 | C | T | synonymous_variant | LOW | c.192C>T|p.Gly64Gly |
S157 S163 |
| 6 | BAA08g12380 | A08 | 10820401 | G | A | missense_variant | MODERATE | c.302G>A|p.Arg101Gln |
S117 |
| 7 | BAA08g12380 | A08 | 10820775 | C | T | missense_variant | MODERATE | c.676C>T|p.Pro226Ser |
S272 |
| 8 | BAA08g12380 | A08 | 10820777 | C | T | synonymous_variant | LOW | c.678C>T|p.Pro226Pro |
S8 |
| 9 | BAA08g12380 | A08 | 10820913 | C | T | missense_variant | MODERATE | c.814C>T|p.Pro272Ser |
S143 S228 |
| 10 | BAA08g12380 | A08 | 10821139 | G | A | stop_gained | HIGH | c.1040G>A|p.Trp347* |
S95 |
| 11 | BAA08g12380 | A08 | 10821179 | C | T | synonymous_variant | LOW | c.1080C>T|p.Ile360Ile |
S296 |
| 12 | BAA08g12380 | A08 | 10821201 | G | A | missense_variant | MODERATE | c.1102G>A|p.Glu368Lys |
S103 |