| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g30500 | A05 | 33535237 | C | T | downstream_gene_variant | MODIFIER | c.*2324G>A| |
S202 |
| 2 | BAA05g30500 | A05 | 33535528 | C | A | downstream_gene_variant | MODIFIER | c.*2033G>T| |
S26 |
| 3 | BAA05g30500 | A05 | 33535626 | G | A | downstream_gene_variant | MODIFIER | c.*1935C>T| |
S218 |
| 4 | BAA05g30500 | A05 | 33535821 | G | A | downstream_gene_variant | MODIFIER | c.*1740C>T| |
S15 S3 |
| 5 | BAA05g30500 | A05 | 33536949 | C | T | downstream_gene_variant | MODIFIER | c.*612G>A| |
S45 |
| 6 | BAA05g30500 | A05 | 33536995 | C | T | downstream_gene_variant | MODIFIER | c.*566G>A| |
S94 |
| 7 | BAA05g30500 | A05 | 33537662 | C | T | missense_variant | MODERATE | c.532G>A|p.Ala178Thr |
S1 |
| 8 | BAA05g30500 | A05 | 33537957 | G | A | synonymous_variant | LOW | c.237C>T|p.Ala79Ala |
S128 S262 |
| 9 | BAA05g30500 | A05 | 33538178 | G | A | missense_variant | MODERATE | c.16C>T|p.Pro6Ser |
S196 |
| 10 | BAA05g30500 | A05 | 33538364 | G | A | upstream_gene_variant | MODIFIER | c.-171C>T| |
S172 S217 |
| 11 | BAA05g30500 | A05 | 33538954 | C | T | upstream_gene_variant | MODIFIER | c.-761G>A| |
S287 |
| 12 | BAA05g30500 | A05 | 33539088 | G | A | upstream_gene_variant | MODIFIER | c.-895C>T| |
S79 S84 |
| 13 | BAA05g30500 | A05 | 33539976 | C | T | upstream_gene_variant | MODIFIER | c.-1783G>A| |
S83 S88 |