Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g15000 | A03 | 6261988 | C | T | missense_variant | MODERATE | c.31C>T|p.Leu11Phe |
S86 |
2 | BAA03g15000 | A03 | 6262467 | C | T | synonymous_variant | LOW | c.510C>T|p.Val170Val |
S134 |
3 | BAA03g15000 | A03 | 6262475 | C | T | missense_variant | MODERATE | c.518C>T|p.Pro173Leu |
S264 |
4 | BAA03g15000 | A03 | 6263175 | C | T | synonymous_variant | LOW | c.1218C>T|p.Gly406Gly |
S134 |
5 | BAA03g15000 | A03 | 6263581 | C | T | missense_variant | MODERATE | c.1624C>T|p.Leu542Phe |
S67 |
6 | BAA03g15000 | A03 | 6263612 | G | A | missense_variant | MODERATE | c.1655G>A|p.Gly552Glu |
S284 |
7 | BAA03g15000 | A03 | 6263690 | G | A | missense_variant | MODERATE | c.1733G>A|p.Gly578Glu |
S75 S81 |
8 | BAA03g15000 | A03 | 6263743 | G | A | missense_variant | MODERATE | c.1786G>A|p.Ala596Thr |
S275 |
9 | BAA03g15000 | A03 | 6264332 | C | T | missense_variant | MODERATE | c.2375C>T|p.Pro792Leu |
S57 |
10 | BAA03g15000 | A03 | 6264344 | T | G | missense_variant | MODERATE | c.2387T>G|p.Phe796Cys |
S204 S239 |
11 | BAA03g15000 | A03 | 6265212 | G | A | downstream_gene_variant | MODIFIER | c.*747G>A| |
S13 S140 |
12 | BAA03g15000 | A03 | 6265579 | C | T | downstream_gene_variant | MODIFIER | c.*1114C>T| |
S85 |
13 | BAA03g15000 | A03 | 6265755 | G | A | downstream_gene_variant | MODIFIER | c.*1290G>A| |
S132 S215 S89 |