| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g00280 | A09 | 373177 | G | A | missense_variant | MODERATE | c.226G>A|p.Ala76Thr |
S78 S83 |
| 2 | BAA09g00280 | A09 | 373260 | C | T | synonymous_variant | LOW | c.309C>T|p.Ser103Ser |
S158 |
| 3 | BAA09g00280 | A09 | 374770 | G | A | missense_variant | MODERATE | c.1819G>A|p.Asp607Asn |
S200 |
| 4 | BAA09g00280 | A09 | 375120 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2100-1G>A| |
S246 |
| 5 | BAA09g00280 | A09 | 375332 | C | T | missense_variant | MODERATE | c.2311C>T|p.Pro771Ser |
S48 |
| 6 | BAA09g00280 | A09 | 375353 | C | T | synonymous_variant | LOW | c.2332C>T|p.Leu778Leu |
S249 |