| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g17880 | A10 | 17016136 | C | T | missense_variant | MODERATE | c.526G>A|p.Ala176Thr |
S23 |
| 2 | BAA10g17880 | A10 | 17016176 | G | A | synonymous_variant | LOW | c.486C>T|p.Tyr162Tyr |
S280 |
| 3 | BAA10g17880 | A10 | 17016482 | C | T | synonymous_variant | LOW | c.180G>A|p.Lys60Lys |
S282 |
| 4 | BAA10g17880 | A10 | 17016659 | C | T | start_lost | HIGH | c.3G>A|p.Met1? |
S195 |
| 5 | BAA10g17880 | A10 | 17016961 | C | T | upstream_gene_variant | MODIFIER | c.-300G>A| |
S108 |
| 6 | BAA10g17880 | A10 | 17017044 | C | T | upstream_gene_variant | MODIFIER | c.-383G>A| |
S122 |
| 7 | BAA10g17880 | A10 | 17017116 | C | T | upstream_gene_variant | MODIFIER | c.-455G>A| |
S96 |
| 8 | BAA10g17880 | A10 | 17021135 | C | T | upstream_gene_variant | MODIFIER | c.-4474G>A| |
S203 |