| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g04560 | A10 | 2323514 | G | A | missense_variant | MODERATE | c.4G>A|p.Asp2Asn |
S230 |
| 2 | BAA10g04560 | A10 | 2323560 | C | T | missense_variant | MODERATE | c.50C>T|p.Ser17Phe |
S143 |
| 3 | BAA10g04560 | A10 | 2323869 | G | A | missense_variant | MODERATE | c.359G>A|p.Gly120Asp |
S18 |
| 4 | BAA10g04560 | A10 | 2325207 | G | A | missense_variant | MODERATE | c.1352G>A|p.Gly451Glu |
S261 |
| 5 | BAA10g04560 | A10 | 2326535 | C | T | synonymous_variant | LOW | c.2286C>T|p.Cys762Cys |
S116 |
| 6 | BAA10g04560 | A10 | 2327551 | G | A | synonymous_variant | LOW | c.2886G>A|p.Arg962Arg |
S105 S106 |
| 7 | BAA10g04560 | A10 | 2328171 | C | T | missense_variant | MODERATE | c.3445C>T|p.Pro1149Ser |
S131 |
| 8 | BAA10g04560 | A10 | 2330336 | C | T | downstream_gene_variant | MODIFIER | c.*2133C>T| |
S88 |