| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00650 | A10 | 318896 | C | T | downstream_gene_variant | MODIFIER | c.*1144G>A| |
S152 |
| 2 | BAA10g00650 | A10 | 319388 | G | A | downstream_gene_variant | MODIFIER | c.*652C>T| |
S236 |
| 3 | BAA10g00650 | A10 | 319684 | G | A | downstream_gene_variant | MODIFIER | c.*356C>T| |
S71 |
| 4 | BAA10g00650 | A10 | 320187 | C | T | synonymous_variant | LOW | c.1299G>A|p.Pro433Pro |
S199 |
| 5 | BAA10g00650 | A10 | 320435 | C | T | missense_variant | MODERATE | c.1051G>A|p.Asp351Asn |
S177 |
| 6 | BAA10g00650 | A10 | 320882 | C | T | missense_variant | MODERATE | c.604G>A|p.Asp202Asn |
S142 |
| 7 | BAA10g00650 | A10 | 321281 | T | C | missense_variant | MODERATE | c.205A>G|p.Thr69Ala |
S240 |
| 8 | BAA10g00650 | A10 | 321844 | C | T | upstream_gene_variant | MODIFIER | c.-359G>A| |
S221 |
| 9 | BAA10g00650 | A10 | 322066 | C | T | upstream_gene_variant | MODIFIER | c.-581G>A| |
S72 |