| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g42500 | A05 | 40231664 | C | A | synonymous_variant | LOW | c.96C>A|p.Thr32Thr |
S132 S89 |
| 2 | BAA05g42500 | A05 | 40231667 | A | T | synonymous_variant | LOW | c.99A>T|p.Gly33Gly |
S132 S89 |
| 3 | BAA05g42500 | A05 | 40231676 | T | C | synonymous_variant | LOW | c.108T>C|p.Asn36Asn |
S132 S89 |
| 4 | BAA05g42500 | A05 | 40231679 | C | G | synonymous_variant | LOW | c.111C>G|p.Leu37Leu |
S132 S89 |
| 5 | BAA05g42500 | A05 | 40231691 | C | T | synonymous_variant | LOW | c.123C>T|p.Ser41Ser |
S132 S89 |
| 6 | BAA05g42500 | A05 | 40231694 | C | G | synonymous_variant | LOW | c.126C>G|p.Val42Val |
S132 S89 |
| 7 | BAA05g42500 | A05 | 40231699 | G | A | missense_variant | MODERATE | c.131G>A|p.Gly44Asp |
S247 |
| 8 | BAA05g42500 | A05 | 40231700 | T | C | synonymous_variant | LOW | c.132T>C|p.Gly44Gly |
S132 S89 |
| 9 | BAA05g42500 | A05 | 40231709 | T | C | synonymous_variant | LOW | c.141T>C|p.Gly47Gly |
S132 S89 |
| 10 | BAA05g42500 | A05 | 40231715 | C | G | synonymous_variant | LOW | c.147C>G|p.Leu49Leu |
S132 S89 |