| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g42180 | A07 | 36702616 | G | A | missense_variant | MODERATE | c.1397C>T|p.Ser466Phe |
S276 |
| 2 | BAA07g42180 | A07 | 36703596 | C | T | missense_variant | MODERATE | c.850G>A|p.Gly284Arg |
S230 |
| 3 | BAA07g42180 | A07 | 36703692 | G | A | synonymous_variant | LOW | c.754C>T|p.Leu252Leu |
S160 |
| 4 | BAA07g42180 | A07 | 36703779 | G | A | synonymous_variant | LOW | c.667C>T|p.Leu223Leu |
S229 |
| 5 | BAA07g42180 | A07 | 36704104 | G | A | synonymous_variant | LOW | c.342C>T|p.Val114Val |
S11 |
| 6 | BAA07g42180 | A07 | 36704290 | G | A | synonymous_variant | LOW | c.156C>T|p.Ser52Ser |
S115 |
| 7 | BAA07g42180 | A07 | 36705383 | C | T | upstream_gene_variant | MODIFIER | c.-938G>A| |
S111 |
| 8 | BAA07g42180 | A07 | 36705459 | C | T | upstream_gene_variant | MODIFIER | c.-1014G>A| |
S114 |
| 9 | BAA07g42180 | A07 | 36707319 | C | T | upstream_gene_variant | MODIFIER | c.-2874G>A| |
S20 |
| 10 | BAA07g42180 | A07 | 36707731 | C | T | upstream_gene_variant | MODIFIER | c.-3286G>A| |
S23 |
| 11 | BAA07g42180 | A07 | 36708277 | C | T | upstream_gene_variant | MODIFIER | c.-3832G>A| |
S295 |