| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g08580 | A10 | 10330123 | C | T | downstream_gene_variant | MODIFIER | c.*134G>A| |
S203 |
| 2 | BAA10g08580 | A10 | 10330195 | C | T | downstream_gene_variant | MODIFIER | c.*62G>A| |
S274 |
| 3 | BAA10g08580 | A10 | 10330220 | G | A | downstream_gene_variant | MODIFIER | c.*37C>T| |
S184 |
| 4 | BAA10g08580 | A10 | 10330358 | C | T | missense_variant | MODERATE | c.379G>A|p.Asp127Asn |
S308 |
| 5 | BAA10g08580 | A10 | 10330377 | C | T | synonymous_variant | LOW | c.360G>A|p.Arg120Arg |
S206 S26 |
| 6 | BAA10g08580 | A10 | 10330660 | C | T | splice_region_variant&intron_variant | LOW | c.161-7G>A| |
S119 |
| 7 | BAA10g08580 | A10 | 10330820 | C | T | synonymous_variant | LOW | c.57G>A|p.Gly19Gly |
S247 |
| 8 | BAA10g08580 | A10 | 10330937 | G | A | upstream_gene_variant | MODIFIER | c.-61C>T| |
S18 |