| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g26800 | A10 | 21104534 | C | T | missense_variant | MODERATE | c.89C>T|p.Ser30Phe |
S115 |
| 2 | BAA10g26800 | A10 | 21104913 | G | A | synonymous_variant | LOW | c.468G>A|p.Gly156Gly |
S216 |
| 3 | BAA10g26800 | A10 | 21105137 | C | T | missense_variant | MODERATE | c.692C>T|p.Ala231Val |
S33 |
| 4 | BAA10g26800 | A10 | 21105242 | C | T | missense_variant | MODERATE | c.797C>T|p.Ala266Val |
S87 |
| 5 | BAA10g26800 | A10 | 21107835 | G | A | downstream_gene_variant | MODIFIER | c.*1614G>A| |
S1 S90 |