Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44850 | A02 | 36812578 | C | T | stop_gained | HIGH | c.3915G>A|p.Trp1305* |
S277 |
2 | BAA02g44850 | A02 | 36812670 | G | A | missense_variant | MODERATE | c.3823C>T|p.Pro1275Ser |
S305 |
3 | BAA02g44850 | A02 | 36812696 | G | A | missense_variant | MODERATE | c.3797C>T|p.Ser1266Phe |
S185 |
4 | BAA02g44850 | A02 | 36812844 | G | A | stop_gained | HIGH | c.3649C>T|p.Gln1217* |
S245 |
5 | BAA02g44850 | A02 | 36813396 | G | A | missense_variant | MODERATE | c.3196C>T|p.Pro1066Ser |
S282 |
6 | BAA02g44850 | A02 | 36816164 | C | T | synonymous_variant | LOW | c.1080G>A|p.Lys360Lys |
S303 |
7 | BAA02g44850 | A02 | 36816559 | C | T | missense_variant | MODERATE | c.685G>A|p.Ala229Thr |
S203 |
8 | BAA02g44850 | A02 | 36821771 | G | A | upstream_gene_variant | MODIFIER | c.-4068C>T| |
S28 |