Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g44130 | A06 | 28322088 | G | A | missense_variant | MODERATE | c.235G>A|p.Val79Ile |
S216 |
2 | BAA06g44130 | A06 | 28322091 | G | A | missense_variant | MODERATE | c.238G>A|p.Ala80Thr |
S305 |
3 | BAA06g44130 | A06 | 28322152 | C | T | missense_variant | MODERATE | c.299C>T|p.Ser100Phe |
S266 |
4 | BAA06g44130 | A06 | 28322489 | G | A | missense_variant | MODERATE | c.475G>A|p.Gly159Arg |
S216 |
5 | BAA06g44130 | A06 | 28323463 | G | A | missense_variant | MODERATE | c.961G>A|p.Glu321Lys |
S209 |
6 | BAA06g44130 | A06 | 28323962 | G | A | missense_variant | MODERATE | c.1210G>A|p.Ala404Thr |
S122 |
7 | BAA06g44130 | A06 | 28324694 | C | T | missense_variant | MODERATE | c.1670C>T|p.Ser557Phe |
S191 |
8 | BAA06g44130 | A06 | 28325128 | G | A | missense_variant | MODERATE | c.2029G>A|p.Ala677Thr |
S115 |