Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g11670 | A06 | 5912575 | G | A | missense_variant | MODERATE | c.365G>A|p.Gly122Glu |
S180 |
2 | BAA06g11670 | A06 | 5913481 | G | A | stop_gained | HIGH | c.1271G>A|p.Trp424* |
S129 |
3 | BAA06g11670 | A06 | 5913673 | G | A | missense_variant | MODERATE | c.1463G>A|p.Arg488Lys |
S291 |
4 | BAA06g11670 | A06 | 5913733 | G | A | missense_variant | MODERATE | c.1523G>A|p.Arg508Lys |
S191 |
5 | BAA06g11670 | A06 | 5913741 | G | A | missense_variant | MODERATE | c.1531G>A|p.Ala511Thr |
S190 |
6 | BAA06g11670 | A06 | 5913860 | G | A | stop_gained | HIGH | c.1650G>A|p.Trp550* |
S7 |
7 | BAA06g11670 | A06 | 5914083 | G | A | missense_variant | MODERATE | c.1873G>A|p.Ala625Thr |
S40 S49 |
8 | BAA06g11670 | A06 | 5914374 | G | A | missense_variant | MODERATE | c.2164G>A|p.Gly722Ser |
S136 |
9 | BAA06g11670 | A06 | 5914611 | G | A | missense_variant | MODERATE | c.2401G>A|p.Asp801Asn |
S272 |
10 | BAA06g11670 | A06 | 5914816 | C | T | missense_variant | MODERATE | c.2606C>T|p.Ser869Phe |
S116 |
11 | BAA06g11670 | A06 | 5915424 | C | T | missense_variant | MODERATE | c.3214C>T|p.Pro1072Ser |
S288 |