| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g31980 | A10 | 23163975 | C | T | missense_variant | MODERATE | c.874G>A|p.Glu292Lys |
S161 |
| 2 | BAA10g31980 | A10 | 23164359 | C | T | missense_variant | MODERATE | c.490G>A|p.Asp164Asn |
S18 |
| 3 | BAA10g31980 | A10 | 23164383 | C | T | missense_variant | MODERATE | c.466G>A|p.Val156Ile |
S301 S304 |
| 4 | BAA10g31980 | A10 | 23164515 | C | T | missense_variant | MODERATE | c.334G>A|p.Ala112Thr |
S139 |
| 5 | BAA10g31980 | A10 | 23164633 | C | T | synonymous_variant | LOW | c.216G>A|p.Gly72Gly |
S11 |
| 6 | BAA10g31980 | A10 | 23164837 | G | A | synonymous_variant | LOW | c.12C>T|p.Tyr4Tyr |
S63 |
| 7 | BAA10g31980 | A10 | 23167886 | C | T | upstream_gene_variant | MODIFIER | c.-3038G>A| |
S281 |
| 8 | BAA10g31980 | A10 | 23168292 | C | T | upstream_gene_variant | MODIFIER | c.-3444G>A| |
S187 |
| 9 | BAA10g31980 | A10 | 23168393 | G | A | upstream_gene_variant | MODIFIER | c.-3545C>T| |
S134 |
| 10 | BAA10g31980 | A10 | 23168953 | G | A | upstream_gene_variant | MODIFIER | c.-4105C>T| |
S183 S198 |