Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g09700 | A03 | 3994562 | C | T | missense_variant | MODERATE | c.2961G>A|p.Met987Ile |
S272 |
2 | BAA03g09700 | A03 | 3995425 | C | T | synonymous_variant | LOW | c.2418G>A|p.Lys806Lys |
S264 |
3 | BAA03g09700 | A03 | 3995538 | C | T | missense_variant | MODERATE | c.2305G>A|p.Glu769Lys |
S205 |
4 | BAA03g09700 | A03 | 3995576 | G | A | missense_variant | MODERATE | c.2267C>T|p.Ser756Phe |
S39 |
5 | BAA03g09700 | A03 | 3995657 | C | T | missense_variant | MODERATE | c.2186G>A|p.Gly729Glu |
S16 |
6 | BAA03g09700 | A03 | 3995708 | C | T | missense_variant | MODERATE | c.2135G>A|p.Arg712Gln |
S58 |
7 | BAA03g09700 | A03 | 3996091 | C | T | synonymous_variant | LOW | c.1752G>A|p.Lys584Lys |
S189 |
8 | BAA03g09700 | A03 | 3996554 | G | A | missense_variant | MODERATE | c.1289C>T|p.Ala430Val |
S224 |
9 | BAA03g09700 | A03 | 3996555 | C | T | missense_variant | MODERATE | c.1288G>A|p.Ala430Thr |
S174 S27 |
10 | BAA03g09700 | A03 | 3996657 | G | A | synonymous_variant | LOW | c.1186C>T|p.Leu396Leu |
S1 S90 |
11 | BAA03g09700 | A03 | 3997079 | G | A | missense_variant | MODERATE | c.764C>T|p.Ser255Phe |
S129 |
12 | BAA03g09700 | A03 | 3997455 | G | A | missense_variant | MODERATE | c.457C>T|p.Pro153Ser |
S261 |
13 | BAA03g09700 | A03 | 3997544 | C | T | missense_variant | MODERATE | c.368G>A|p.Ser123Asn |
S28 |