Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g42130 | A03 | 19868871 | G | A | synonymous_variant | LOW | c.555G>A|p.Glu185Glu |
S177 |
2 | BAA03g42130 | A03 | 19869463 | C | T | missense_variant | MODERATE | c.1147C>T|p.Pro383Ser |
S19 S208 S93 |
3 | BAA03g42130 | A03 | 19869561 | G | A | synonymous_variant | LOW | c.1245G>A|p.Lys415Lys |
S303 |
4 | BAA03g42130 | A03 | 19869589 | G | A | splice_donor_variant&intron_variant | HIGH | c.1272+1G>A| |
S261 |
5 | BAA03g42130 | A03 | 19869852 | G | A | missense_variant | MODERATE | c.1453G>A|p.Glu485Lys |
S5 |
6 | BAA03g42130 | A03 | 19869988 | G | A | missense_variant | MODERATE | c.1589G>A|p.Gly530Glu |
S178 |
7 | BAA03g42130 | A03 | 19870048 | G | A | missense_variant | MODERATE | c.1649G>A|p.Arg550Lys |
S20 |
8 | BAA03g42130 | A03 | 19870378 | C | T | missense_variant | MODERATE | c.1979C>T|p.Thr660Met |
S135 S273 |
9 | BAA03g42130 | A03 | 19870789 | C | T | stop_gained | HIGH | c.2317C>T|p.Gln773* |
S159 S243 |