| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00050 | A10 | 15080 | C | T | splice_region_variant&intron_variant | LOW | c.1313+5G>A| |
S132 S137 S237 |
| 2 | BAA10g00050 | A10 | 15723 | G | A | missense_variant | MODERATE | c.1037C>T|p.Thr346Met |
S293 |
| 3 | BAA10g00050 | A10 | 15863 | C | T | missense_variant | MODERATE | c.989G>A|p.Ser330Asn |
S266 |
| 4 | BAA10g00050 | A10 | 16822 | C | T | missense_variant | MODERATE | c.583G>A|p.Gly195Ser |
S116 |
| 5 | BAA10g00050 | A10 | 21278 | C | T | upstream_gene_variant | MODIFIER | c.-3132G>A| |
S135 |
| 6 | BAA10g00050 | A10 | 21448 | C | T | upstream_gene_variant | MODIFIER | c.-3302G>A| |
S265 |
| 7 | BAA10g00050 | A10 | 22885 | G | A | upstream_gene_variant | MODIFIER | c.-4739C>T| |
S76 |