| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g09190 | A10 | 11221873 | G | A | upstream_gene_variant | MODIFIER | c.-1699G>A| |
S286 |
| 2 | BAA10g09190 | A10 | 11223609 | C | T | missense_variant | MODERATE | c.38C>T|p.Pro13Leu |
S68 |
| 3 | BAA10g09190 | A10 | 11223692 | C | T | missense_variant | MODERATE | c.121C>T|p.Arg41Cys |
S308 |
| 4 | BAA10g09190 | A10 | 11224804 | G | A | missense_variant | MODERATE | c.931G>A|p.Ala311Thr |
S245 |
| 5 | BAA10g09190 | A10 | 11224815 | G | A | synonymous_variant | LOW | c.942G>A|p.Lys314Lys |
S9 |
| 6 | BAA10g09190 | A10 | 11224970 | C | T | splice_region_variant&intron_variant | LOW | c.1006-7C>T| |
S153 S213 |
| 7 | BAA10g09190 | A10 | 11225236 | C | T | missense_variant | MODERATE | c.1172C>T|p.Ala391Val |
S174 S27 |