| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00040 | A10 | 13709 | C | T | missense_variant | MODERATE | c.667G>A|p.Asp223Asn |
S143 |
| 2 | BAA10g00040 | A10 | 13932 | G | A | synonymous_variant | LOW | c.444C>T|p.Val148Val |
S134 |
| 3 | BAA10g00040 | A10 | 14401 | G | A | missense_variant | MODERATE | c.41C>T|p.Ala14Val |
S278 |
| 4 | BAA10g00040 | A10 | 17765 | G | A | upstream_gene_variant | MODIFIER | c.-3324C>T| |
S80 |
| 5 | BAA10g00040 | A10 | 19426 | G | A | upstream_gene_variant | MODIFIER | c.-4985C>T| |
S301 S304 |