Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18230 | A08 | 14656009 | G | A | synonymous_variant | LOW | c.747G>A|p.Lys249Lys |
S282 |
2 | BAA08g18230 | A08 | 14656649 | C | T | synonymous_variant | LOW | c.1287C>T|p.Leu429Leu |
S105 S106 |
3 | BAA08g18230 | A08 | 14657073 | G | A | missense_variant | MODERATE | c.1711G>A|p.Glu571Lys |
S100 |
4 | BAA08g18230 | A08 | 14657127 | C | T | missense_variant | MODERATE | c.1765C>T|p.Leu589Phe |
S166 |
5 | BAA08g18230 | A08 | 14657756 | C | T | synonymous_variant | LOW | c.2394C>T|p.His798His |
S244 |
6 | BAA08g18230 | A08 | 14658310 | C | T | synonymous_variant | LOW | c.2610C>T|p.Leu870Leu |
S305 |
7 | BAA08g18230 | A08 | 14658696 | C | T | missense_variant | MODERATE | c.2900C>T|p.Thr967Ile |
S270 |
8 | BAA08g18230 | A08 | 14658715 | G | A | synonymous_variant | LOW | c.2919G>A|p.Lys973Lys |
S280 |
9 | BAA08g18230 | A08 | 14658957 | C | T | missense_variant | MODERATE | c.3032C>T|p.Ala1011Val |
S215 |