| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g28910 | A05 | 32627488 | C | T | upstream_gene_variant | MODIFIER | c.-2195C>T| |
S162 |
| 2 | BAA05g28910 | A05 | 32628161 | G | A | upstream_gene_variant | MODIFIER | c.-1522G>A| |
S252 |
| 3 | BAA05g28910 | A05 | 32630249 | C | T | missense_variant | MODERATE | c.457C>T|p.Pro153Ser |
S63 |
| 4 | BAA05g28910 | A05 | 32630632 | G | A | missense_variant | MODERATE | c.840G>A|p.Met280Ile |
S239 |
| 5 | BAA05g28910 | A05 | 32630736 | G | A | missense_variant | MODERATE | c.944G>A|p.Arg315Lys |
S124 |
| 6 | BAA05g28910 | A05 | 32630737 | G | A | synonymous_variant | LOW | c.945G>A|p.Arg315Arg |
S109 |
| 7 | BAA05g28910 | A05 | 32630763 | C | T | missense_variant | MODERATE | c.971C>T|p.Ala324Val |
S25 |
| 8 | BAA05g28910 | A05 | 32630788 | G | A | synonymous_variant | LOW | c.996G>A|p.Lys332Lys |
S160 |
| 9 | BAA05g28910 | A05 | 32631556 | G | A | splice_region_variant&synonymous_variant | LOW | c.1245G>A|p.Glu415Glu |
S138 |
| 10 | BAA05g28910 | A05 | 32632171 | C | T | splice_region_variant&intron_variant | LOW | c.1338-3C>T| |
S73 S91 |
| 11 | BAA05g28910 | A05 | 32632207 | G | A | synonymous_variant | LOW | c.1371G>A|p.Gln457Gln |
S205 |
| 12 | BAA05g28910 | A05 | 32632730 | C | T | missense_variant | MODERATE | c.1763C>T|p.Ser588Phe |
S276 |
| 13 | BAA05g28910 | A05 | 32632906 | C | T | missense_variant | MODERATE | c.1939C>T|p.Pro647Ser |
S115 |
| 14 | BAA05g28910 | A05 | 32634154 | G | A | missense_variant | MODERATE | c.2582G>A|p.Arg861His |
S257 |
| 15 | BAA05g28910 | A05 | 32635056 | C | T | missense_variant | MODERATE | c.2980C>T|p.Pro994Ser |
S192 |
| 16 | BAA05g28910 | A05 | 32635563 | G | A | missense_variant&splice_region_variant | MODERATE | c.3328G>A|p.Glu1110Lys |
S257 |
| 17 | BAA05g28910 | A05 | 32636851 | C | T | downstream_gene_variant | MODIFIER | c.*412C>T| |
S181 |
| 18 | BAA05g28910 | A05 | 32637320 | G | A | downstream_gene_variant | MODIFIER | c.*881G>A| |
S95 |