| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g16530 | A08 | 13671233 | G | A | missense_variant | MODERATE | c.371G>A|p.Gly124Asp |
S34 |
| 2 | BAA08g16530 | A08 | 13672062 | G | A | synonymous_variant | LOW | c.693G>A|p.Glu231Glu |
S181 |
| 3 | BAA08g16530 | A08 | 13672564 | G | A | missense_variant | MODERATE | c.1195G>A|p.Glu399Lys |
S100 |
| 4 | BAA08g16530 | A08 | 13672679 | C | T | missense_variant | MODERATE | c.1310C>T|p.Thr437Ile |
S180 |
| 5 | BAA08g16530 | A08 | 13673974 | G | A | intron_variant | MODIFIER | c.1717+662G>A| |
S12 |
| 6 | BAA08g16530 | A08 | 13674739 | G | A | intron_variant | MODIFIER | c.1718-377G>A| |
S132 S137 S89 |
| 7 | BAA08g16530 | A08 | 13675565 | C | T | stop_gained | HIGH | c.2002C>T|p.Gln668* |
S80 |
| 8 | BAA08g16530 | A08 | 13676194 | G | A | missense_variant | MODERATE | c.2299G>A|p.Val767Ile |
S133 |
| 9 | BAA08g16530 | A08 | 13676421 | G | A | synonymous_variant | LOW | c.2526G>A|p.Gly842Gly |
S95 |