| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g50790 | A09 | 53494575 | C | T | missense_variant | MODERATE | c.76C>T|p.His26Tyr |
S237 |
| 2 | BAA09g50790 | A09 | 53494943 | G | A | synonymous_variant | LOW | c.444G>A|p.Glu148Glu |
S135 |
| 3 | BAA09g50790 | A09 | 53496154 | G | A | synonymous_variant | LOW | c.1083G>A|p.Val361Val |
S65 |
| 4 | BAA09g50790 | A09 | 53496422 | G | A | missense_variant | MODERATE | c.1279G>A|p.Asp427Asn |
S262 |
| 5 | BAA09g50790 | A09 | 53496653 | C | T | synonymous_variant | LOW | c.1431C>T|p.Asn477Asn |
S224 |
| 6 | BAA09g50790 | A09 | 53496712 | C | T | missense_variant | MODERATE | c.1490C>T|p.Ala497Val |
S180 |
| 7 | BAA09g50790 | A09 | 53496893 | C | T | synonymous_variant | LOW | c.1671C>T|p.Asp557Asp |
S103 |
| 8 | BAA09g50790 | A09 | 53497055 | G | A | splice_region_variant&stop_retained_variant | LOW | c.1833G>A|p.Ter611Ter |
S247 |