Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41720 | A01 | 27724626 | G | A | missense_variant | MODERATE | c.59G>A|p.Gly20Glu |
S138 |
2 | BAA01g41720 | A01 | 27724718 | G | A | missense_variant | MODERATE | c.151G>A|p.Glu51Lys |
S71 |
3 | BAA01g41720 | A01 | 27725000 | C | T | missense_variant | MODERATE | c.433C>T|p.His145Tyr |
S240 |
4 | BAA01g41720 | A01 | 27725018 | G | A | missense_variant | MODERATE | c.451G>A|p.Ala151Thr |
S25 |
5 | BAA01g41720 | A01 | 27725675 | C | T | missense_variant | MODERATE | c.1108C>T|p.His370Tyr |
S292 |
6 | BAA01g41720 | A01 | 27725867 | G | A | missense_variant&splice_region_variant | MODERATE | c.1300G>A|p.Glu434Lys |
S197 |
7 | BAA01g41720 | A01 | 27727292 | C | T | missense_variant | MODERATE | c.1894C>T|p.Pro632Ser |
S301 S304 |
8 | BAA01g41720 | A01 | 27727363 | G | A | synonymous_variant | LOW | c.1965G>A|p.Gly655Gly |
S294 |
9 | BAA01g41720 | A01 | 27727984 | C | T | synonymous_variant | LOW | c.2586C>T|p.Leu862Leu |
S88 |
10 | BAA01g41720 | A01 | 27730100 | C | T | downstream_gene_variant | MODIFIER | c.*1894C>T| |
S156 |
11 | BAA01g41720 | A01 | 27730691 | C | T | downstream_gene_variant | MODIFIER | c.*2485C>T| |
S247 |
12 | BAA01g41720 | A01 | 27731291 | G | A | downstream_gene_variant | MODIFIER | c.*3085G>A| |
S70 |
13 | BAA01g41720 | A01 | 27732349 | C | T | downstream_gene_variant | MODIFIER | c.*4143C>T| |
S69 |