Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37840 | A02 | 32373217 | C | T | missense_variant | MODERATE | c.41C>T|p.Ser14Phe |
S165 |
2 | BAA02g37840 | A02 | 32373481 | C | T | missense_variant | MODERATE | c.305C>T|p.Thr102Ile |
S270 |
3 | BAA02g37840 | A02 | 32374549 | C | T | missense_variant | MODERATE | c.1373C>T|p.Thr458Ile |
S109 |
4 | BAA02g37840 | A02 | 32374744 | C | T | missense_variant | MODERATE | c.1568C>T|p.Ser523Leu |
S49 |
5 | BAA02g37840 | A02 | 32374864 | G | A | missense_variant | MODERATE | c.1688G>A|p.Gly563Glu |
S217 S248 |
6 | BAA02g37840 | A02 | 32374877 | G | A | synonymous_variant | LOW | c.1701G>A|p.Val567Val |
S164 |
7 | BAA02g37840 | A02 | 32377392 | C | T | downstream_gene_variant | MODIFIER | c.*2032C>T| |
S152 |
8 | BAA02g37840 | A02 | 32377531 | G | A | downstream_gene_variant | MODIFIER | c.*2171G>A| |
S150 |
9 | BAA02g37840 | A02 | 32377997 | C | T | downstream_gene_variant | MODIFIER | c.*2637C>T| |
S305 |
10 | BAA02g37840 | A02 | 32378679 | C | T | downstream_gene_variant | MODIFIER | c.*3319C>T| |
S263 |
11 | BAA02g37840 | A02 | 32378749 | C | T | downstream_gene_variant | MODIFIER | c.*3389C>T| |
S138 |