Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g30880 | A03 | 14493738 | G | A | missense_variant | MODERATE | c.55G>A|p.Gly19Ser |
S10 |
2 | BAA03g30880 | A03 | 14494619 | G | A | synonymous_variant | LOW | c.936G>A|p.Ser312Ser |
S195 |
3 | BAA03g30880 | A03 | 14494730 | C | T | synonymous_variant | LOW | c.1047C>T|p.Asp349Asp |
S263 |
4 | BAA03g30880 | A03 | 14495074 | G | A | missense_variant | MODERATE | c.1391G>A|p.Gly464Asp |
S63 |
5 | BAA03g30880 | A03 | 14495110 | G | A | missense_variant | MODERATE | c.1427G>A|p.Gly476Glu |
S157 S167 S236 S257 |
6 | BAA03g30880 | A03 | 14495148 | G | A | missense_variant | MODERATE | c.1465G>A|p.Glu489Lys |
S143 |
7 | BAA03g30880 | A03 | 14495165 | C | T | synonymous_variant | LOW | c.1482C>T|p.Asp494Asp |
S131 |
8 | BAA03g30880 | A03 | 14495372 | G | A | stop_gained | HIGH | c.1689G>A|p.Trp563* |
S209 |
9 | BAA03g30880 | A03 | 14495399 | G | A | synonymous_variant | LOW | c.1716G>A|p.Gly572Gly |
S276 |