| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g09990 | A10 | 11794753 | C | T | missense_variant | MODERATE | c.89C>T|p.Ser30Phe |
S273 |
| 2 | BAA10g09990 | A10 | 11794769 | C | T | synonymous_variant | LOW | c.105C>T|p.Asn35Asn |
S294 |
| 3 | BAA10g09990 | A10 | 11795519 | G | A | downstream_gene_variant | MODIFIER | c.*144G>A| |
S262 |
| 4 | BAA10g09990 | A10 | 11797006 | C | T | downstream_gene_variant | MODIFIER | c.*1631C>T| |
S174 |
| 5 | BAA10g09990 | A10 | 11797012 | C | A | downstream_gene_variant | MODIFIER | c.*1637C>A| |
S23 S294 |
| 6 | BAA10g09990 | A10 | 11797572 | G | A | downstream_gene_variant | MODIFIER | c.*2197G>A| |
S192 |
| 7 | BAA10g09990 | A10 | 11798403 | C | T | downstream_gene_variant | MODIFIER | c.*3028C>T| |
S10 |
| 8 | BAA10g09990 | A10 | 11798479 | C | T | downstream_gene_variant | MODIFIER | c.*3104C>T| |
S241 |