Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g19340 | A05 | 11375566 | G | A | missense_variant | MODERATE | c.280G>A|p.Glu94Lys |
S4 |
2 | BAA05g19340 | A05 | 11375860 | G | A | missense_variant | MODERATE | c.574G>A|p.Glu192Lys |
S218 |
3 | BAA05g19340 | A05 | 11376005 | G | A | missense_variant | MODERATE | c.719G>A|p.Gly240Glu |
S139 |
4 | BAA05g19340 | A05 | 11376139 | G | A | missense_variant | MODERATE | c.853G>A|p.Val285Ile |
S236 |
5 | BAA05g19340 | A05 | 11376392 | C | T | missense_variant | MODERATE | c.1106C>T|p.Ala369Val |
S63 |
6 | BAA05g19340 | A05 | 11376493 | G | A | missense_variant | MODERATE | c.1207G>A|p.Glu403Lys |
S296 |
7 | BAA05g19340 | A05 | 11376587 | C | T | missense_variant | MODERATE | c.1301C>T|p.Ser434Phe |
S133 |
8 | BAA05g19340 | A05 | 11376769 | G | A | missense_variant | MODERATE | c.1483G>A|p.Val495Ile |
S282 |
9 | BAA05g19340 | A05 | 11376791 | G | A | missense_variant | MODERATE | c.1505G>A|p.Gly502Glu |
S246 |
10 | BAA05g19340 | A05 | 11376797 | C | T | missense_variant | MODERATE | c.1511C>T|p.Pro504Leu |
S146 |
11 | BAA05g19340 | A05 | 11376872 | C | T | missense_variant | MODERATE | c.1586C>T|p.Ser529Phe |
S162 |