| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g41160 | A09 | 47963123 | G | A | upstream_gene_variant | MODIFIER | c.-4303G>A| |
S107 |
| 2 | BAA09g41160 | A09 | 47963164 | G | A | upstream_gene_variant | MODIFIER | c.-4262G>A| |
S246 |
| 3 | BAA09g41160 | A09 | 47963338 | C | T | upstream_gene_variant | MODIFIER | c.-4088C>T| |
S303 |
| 4 | BAA09g41160 | A09 | 47964172 | C | T | upstream_gene_variant | MODIFIER | c.-3254C>T| |
S61 |
| 5 | BAA09g41160 | A09 | 47964244 | C | T | upstream_gene_variant | MODIFIER | c.-3182C>T| |
S212 |
| 6 | BAA09g41160 | A09 | 47964246 | C | T | upstream_gene_variant | MODIFIER | c.-3180C>T| |
S174 |
| 7 | BAA09g41160 | A09 | 47965959 | C | A | upstream_gene_variant | MODIFIER | c.-1467C>A| |
S221 |
| 8 | BAA09g41160 | A09 | 47966356 | C | T | upstream_gene_variant | MODIFIER | c.-1070C>T| |
S129 |
| 9 | BAA09g41160 | A09 | 47968007 | C | A | synonymous_variant | LOW | c.582C>A|p.Ser194Ser |
S240 |
| 10 | BAA09g41160 | A09 | 47968305 | G | A | missense_variant | MODERATE | c.880G>A|p.Glu294Lys |
S217 S248 |
| 11 | BAA09g41160 | A09 | 47968389 | G | A | missense_variant | MODERATE | c.964G>A|p.Ala322Thr |
S164 |
| 12 | BAA09g41160 | A09 | 47968515 | G | A | missense_variant | MODERATE | c.1090G>A|p.Val364Ile |
S78 S83 |
| 13 | BAA09g41160 | A09 | 47968834 | C | T | downstream_gene_variant | MODIFIER | c.*257C>T| |
S174 S27 |
| 14 | BAA09g41160 | A09 | 47969447 | T | C | downstream_gene_variant | MODIFIER | c.*870T>C| |
S223 |
| 15 | BAA09g41160 | A09 | 47969883 | C | T | downstream_gene_variant | MODIFIER | c.*1306C>T| |
S37 |
| 16 | BAA09g41160 | A09 | 47970204 | C | T | downstream_gene_variant | MODIFIER | c.*1627C>T| |
S157 S163 |
| 17 | BAA09g41160 | A09 | 47971391 | C | T | downstream_gene_variant | MODIFIER | c.*2814C>T| |
S296 |
| 18 | BAA09g41160 | A09 | 47972190 | C | T | downstream_gene_variant | MODIFIER | c.*3613C>T| |
S138 |