| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 42751 | BAA01g26400 | A01 | 14699835 | C | T | downstream_gene_variant | MODIFIER | c.*3283C>T| |
S286 |
| 42752 | BAA01g26400 | A01 | 14700601 | C | T | downstream_gene_variant | MODIFIER | c.*4049C>T| |
S53 |
| 42753 | BAA01g26400-BAA01g26410 | A01 | 14701674 | G | A | intergenic_region | MODIFIER | n.14701674G>A| |
S263 |
| 42754 | BAA01g26410 | A01 | 14703810 | C | T | downstream_gene_variant | MODIFIER | c.*4795G>A| |
S136 |
| 42755 | BAA01g26410 | A01 | 14703852 | C | T | downstream_gene_variant | MODIFIER | c.*4753G>A| |
S203 |
| 42756 | BAA01g26410 | A01 | 14704914 | C | T | downstream_gene_variant | MODIFIER | c.*3691G>A| |
S107 |
| 42757 | BAA01g26410 | A01 | 14705341 | C | T | downstream_gene_variant | MODIFIER | c.*3264G>A| |
S270 |
| 42758 | BAA01g26410 | A01 | 14705404 | G | A | downstream_gene_variant | MODIFIER | c.*3201C>T| |
S244 |
| 42759 | BAA01g26410 | A01 | 14705499 | G | A | downstream_gene_variant | MODIFIER | c.*3106C>T| |
S169 |
| 42760 | BAA01g26410 | A01 | 14705999 | C | T | downstream_gene_variant | MODIFIER | c.*2606G>A| |
S264 |
| 42761 | BAA01g26410 | A01 | 14707398 | C | T | downstream_gene_variant | MODIFIER | c.*1207G>A| |
S242 |
| 42762 | BAA01g26410 | A01 | 14707802 | G | T | downstream_gene_variant | MODIFIER | c.*803C>A| |
S20 |
| 42763 | BAA01g26410 | A01 | 14708409 | C | A | downstream_gene_variant | MODIFIER | c.*196G>T| |
S143 |
| 42764 | BAA01g26410 | A01 | 14708423 | G | A | downstream_gene_variant | MODIFIER | c.*182C>T| |
S236 |
| 42765 | BAA01g26410 | A01 | 14708483 | G | A | downstream_gene_variant | MODIFIER | c.*122C>T| |
S170 |
| 42766 | BAA01g26410 | A01 | 14708847 | C | T | missense_variant | MODERATE | c.979G>A|p.Gly327Arg |
S237 |
| 42767 | BAA01g26410 | A01 | 14709326 | G | A | intron_variant | MODIFIER | c.686-34C>T| |
S79 S91 |
| 42768 | BAA01g26410 | A01 | 14709969 | C | T | intron_variant | MODIFIER | c.686-677G>A| |
S104 S52 |
| 42769 | BAA01g26410 | A01 | 14710116 | C | T | intron_variant | MODIFIER | c.686-824G>A| |
S286 |
| 42770 | BAA01g26410 | A01 | 14710497 | G | A | intron_variant | MODIFIER | c.685+452C>T| |
S67 |
| 42771 | BAA01g26410 | A01 | 14710537 | G | A | intron_variant | MODIFIER | c.685+412C>T| |
S34 |
| 42772 | BAA01g26410 | A01 | 14710692 | G | A | intron_variant | MODIFIER | c.685+257C>T| |
S126 |
| 42773 | BAA01g26410 | A01 | 14711585 | C | T | missense_variant | MODERATE | c.49G>A|p.Val17Met |
S114 |
| 42774 | BAA01g26410 | A01 | 14712063 | C | T | upstream_gene_variant | MODIFIER | c.-430G>A| |
S277 |
| 42775 | BAA01g26410 | A01 | 14714094 | C | T | upstream_gene_variant | MODIFIER | c.-2461G>A| |
S36 |