| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g01090 | A10 | 546052 | G | A | downstream_gene_variant | MODIFIER | c.*3425C>T| |
S263 |
| 2 | BAA10g01090 | A10 | 546409 | C | T | downstream_gene_variant | MODIFIER | c.*3068G>A| |
S287 |
| 3 | BAA10g01090 | A10 | 550127 | C | T | missense_variant | MODERATE | c.736G>A|p.Asp246Asn |
S259 |
| 4 | BAA10g01090 | A10 | 550360 | G | A | missense_variant | MODERATE | c.571C>T|p.His191Tyr |
S228 |
| 5 | BAA10g01090 | A10 | 551210 | G | A | upstream_gene_variant | MODIFIER | c.-107C>T| |
S241 |
| 6 | BAA10g01090 | A10 | 551558 | C | A | upstream_gene_variant | MODIFIER | c.-455G>T| |
S172 S260 S281 S283 S61 |
| 7 | BAA10g01090 | A10 | 551895 | G | A | upstream_gene_variant | MODIFIER | c.-792C>T| |
S280 |
| 8 | BAA10g01090 | A10 | 553908 | G | A | upstream_gene_variant | MODIFIER | c.-2805C>T| |
S167 |
| 9 | BAA10g01090 | A10 | 554333 | G | A | upstream_gene_variant | MODIFIER | c.-3230C>T| |
S33 |
| 10 | BAA10g01090 | A10 | 555502 | G | A | upstream_gene_variant | MODIFIER | c.-4399C>T| |
S48 |