Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12790 | A01 | 6051382 | G | A | missense_variant | MODERATE | c.211G>A|p.Ala71Thr |
S174 |
2 | BAA01g12790 | A01 | 6051707 | G | A | missense_variant | MODERATE | c.536G>A|p.Gly179Glu |
S34 |
3 | BAA01g12790 | A01 | 6052056 | C | T | synonymous_variant | LOW | c.885C>T|p.Tyr295Tyr |
S305 |
4 | BAA01g12790 | A01 | 6052705 | C | T | stop_gained | HIGH | c.1444C>T|p.Gln482* |
S148 S210 S30 S31 |
5 | BAA01g12790 | A01 | 6052868 | C | T | missense_variant | MODERATE | c.1607C>T|p.Ser536Phe |
S260 |
6 | BAA01g12790 | A01 | 6053002 | C | T | synonymous_variant | LOW | c.1741C>T|p.Leu581Leu |
S128 |
7 | BAA01g12790 | A01 | 6053346 | C | T | synonymous_variant | LOW | c.2085C>T|p.Gly695Gly |
S100 |
8 | BAA01g12790 | A01 | 6053506 | G | A | missense_variant | MODERATE | c.2245G>A|p.Glu749Lys |
S292 |
9 | BAA01g12790 | A01 | 6053785 | G | A | missense_variant | MODERATE | c.2524G>A|p.Asp842Asn |
S262 |
10 | BAA01g12790 | A01 | 6054048 | G | A | missense_variant | MODERATE | c.2707G>A|p.Gly903Arg |
S28 |
11 | BAA01g12790 | A01 | 6057691 | C | T | downstream_gene_variant | MODIFIER | c.*3197C>T| |
S107 |
12 | BAA01g12790 | A01 | 6057866 | C | T | downstream_gene_variant | MODIFIER | c.*3372C>T| |
S161 |