| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA04g17580 | A04 | 21758291 | C | T | upstream_gene_variant | MODIFIER | c.-3722C>T| |
S152 |
| 2 | BAA04g17580 | A04 | 21760253 | G | A | upstream_gene_variant | MODIFIER | c.-1760G>A| |
S153 S257 |
| 3 | BAA04g17580 | A04 | 21760386 | G | A | upstream_gene_variant | MODIFIER | c.-1627G>A| |
S234 |
| 4 | BAA04g17580 | A04 | 21760559 | C | T | upstream_gene_variant | MODIFIER | c.-1454C>T| |
S8 |
| 5 | BAA04g17580 | A04 | 21760854 | G | A | upstream_gene_variant | MODIFIER | c.-1159G>A| |
S153 S213 |
| 6 | BAA04g17580 | A04 | 21761186 | C | T | upstream_gene_variant | MODIFIER | c.-827C>T| |
S308 |
| 7 | BAA04g17580 | A04 | 21761760 | G | A | upstream_gene_variant | MODIFIER | c.-253G>A| |
S160 |
| 8 | BAA04g17580 | A04 | 21762908 | C | T | intron_variant | MODIFIER | c.703-21C>T| |
S117 |
| 9 | BAA04g17580 | A04 | 21763359 | G | A | missense_variant | MODERATE | c.1042G>A|p.Glu348Lys |
S171 |
| 10 | BAA04g17580 | A04 | 21763422 | C | T | missense_variant | MODERATE | c.1105C>T|p.Pro369Ser |
S243 S299 |
| 11 | BAA04g17580 | A04 | 21763657 | G | A | missense_variant | MODERATE | c.1340G>A|p.Gly447Glu |
S251 |
| 12 | BAA04g17580 | A04 | 21764088 | C | T | synonymous_variant | LOW | c.1771C>T|p.Leu591Leu |
S64 |
| 13 | BAA04g17580 | A04 | 21765189 | G | A | missense_variant | MODERATE | c.2872G>A|p.Asp958Asn |
S11 |
| 14 | BAA04g17580 | A04 | 21765876 | G | A | synonymous_variant | LOW | c.3483G>A|p.Gly1161Gly |
S13 |
| 15 | BAA04g17580 | A04 | 21766170 | C | T | intron_variant | MODIFIER | c.3655-30C>T| |
S187 |
| 16 | BAA04g17580 | A04 | 21766721 | C | T | intron_variant | MODIFIER | c.3984+17C>T| |
S200 |
| 17 | BAA04g17580 | A04 | 21768663 | G | A | downstream_gene_variant | MODIFIER | c.*1759G>A| |
S233 |
| 18 | BAA04g17580 | A04 | 21770104 | C | T | downstream_gene_variant | MODIFIER | c.*3200C>T| |
S126 S61 |
| 19 | BAA04g17580 | A04 | 21771895 | G | A | downstream_gene_variant | MODIFIER | c.*4991G>A| |
S166 |