| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g02130 | A05 | 1160354 | C | T | upstream_gene_variant | MODIFIER | c.-3204C>T| |
S249 |
| 2 | BAA05g02130 | A05 | 1163574 | G | A | missense_variant | MODERATE | c.17G>A|p.Ser6Asn |
S212 |
| 3 | BAA05g02130 | A05 | 1164054 | C | T | missense_variant | MODERATE | c.497C>T|p.Ala166Val |
S288 |
| 4 | BAA05g02130 | A05 | 1164201 | G | A | missense_variant | MODERATE | c.644G>A|p.Gly215Glu |
S221 |
| 5 | BAA05g02130 | A05 | 1164329 | G | A | missense_variant | MODERATE | c.772G>A|p.Gly258Arg |
S192 |
| 6 | BAA05g02130 | A05 | 1164880 | G | A | missense_variant | MODERATE | c.1204G>A|p.Ala402Thr |
S158 |
| 7 | BAA05g02130 | A05 | 1166516 | C | T | synonymous_variant | LOW | c.2298C>T|p.Phe766Phe |
S267 |
| 8 | BAA05g02130 | A05 | 1167079 | G | A | downstream_gene_variant | MODIFIER | c.*539G>A| |
S129 |
| 9 | BAA05g02130 | A05 | 1167621 | C | T | downstream_gene_variant | MODIFIER | c.*1081C>T| |
S115 |