Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g35000 | A05 | 35887528 | G | A | missense_variant | MODERATE | c.443G>A|p.Cys148Tyr |
S149 |
2 | BAA05g35000 | A05 | 35888220 | C | T | synonymous_variant | LOW | c.579C>T|p.Phe193Phe |
S53 |
3 | BAA05g35000 | A05 | 35888428 | G | A | missense_variant | MODERATE | c.670G>A|p.Val224Met |
S156 S303 |
4 | BAA05g35000 | A05 | 35888801 | G | A | missense_variant | MODERATE | c.736G>A|p.Glu246Lys |
S291 |
5 | BAA05g35000 | A05 | 35889215 | C | T | synonymous_variant | LOW | c.921C>T|p.Val307Val |
S115 |
6 | BAA05g35000 | A05 | 35889413 | G | A | missense_variant | MODERATE | c.1033G>A|p.Val345Ile |
S224 |
7 | BAA05g35000 | A05 | 35889452 | G | A | splice_donor_variant&intron_variant | HIGH | c.1071+1G>A| |
S279 |
8 | BAA05g35000 | A05 | 35889621 | G | A | synonymous_variant | LOW | c.1149G>A|p.Leu383Leu |
S252 |
9 | BAA05g35000 | A05 | 35893696 | G | A | downstream_gene_variant | MODIFIER | c.*4051G>A| |
S40 S49 |