Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g48540 | A03 | 23326095 | G | A | missense_variant | MODERATE | c.217G>A|p.Glu73Lys |
S25 |
2 | BAA03g48540 | A03 | 23326137 | G | A | missense_variant | MODERATE | c.259G>A|p.Glu87Lys |
S34 |
3 | BAA03g48540 | A03 | 23326202 | C | T | synonymous_variant | LOW | c.324C>T|p.His108His |
S82 S92 |
4 | BAA03g48540 | A03 | 23326448 | G | A | synonymous_variant | LOW | c.570G>A|p.Arg190Arg |
S34 |
5 | BAA03g48540 | A03 | 23326938 | C | T | synonymous_variant | LOW | c.981C>T|p.Ile327Ile |
S92 |
6 | BAA03g48540 | A03 | 23327263 | G | A | missense_variant | MODERATE | c.1306G>A|p.Val436Ile |
S195 |
7 | BAA03g48540 | A03 | 23327336 | G | A | stop_gained | HIGH | c.1379G>A|p.Trp460* |
S260 |
8 | BAA03g48540 | A03 | 23327689 | G | A | missense_variant | MODERATE | c.1732G>A|p.Asp578Asn |
S1 S90 |
9 | BAA03g48540 | A03 | 23328391 | C | T | synonymous_variant | LOW | c.2434C>T|p.Leu812Leu |
S149 |
10 | BAA03g48540 | A03 | 23328479 | C | T | missense_variant | MODERATE | c.2455C>T|p.Pro819Ser |
S202 |
11 | BAA03g48540 | A03 | 23328576 | G | A | missense_variant | MODERATE | c.2552G>A|p.Gly851Glu |
S224 |