Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44130 | A01 | 29265528 | C | T | upstream_gene_variant | MODIFIER | c.-3162C>T| |
S47 |
2 | BAA01g44130 | A01 | 29265633 | C | T | upstream_gene_variant | MODIFIER | c.-3057C>T| |
S206 S26 |
3 | BAA01g44130 | A01 | 29269395 | G | A | missense_variant | MODERATE | c.616G>A|p.Gly206Ser |
S80 |
4 | BAA01g44130 | A01 | 29269758 | G | A | missense_variant | MODERATE | c.712G>A|p.Glu238Lys |
S194 |
5 | BAA01g44130 | A01 | 29269850 | C | T | synonymous_variant | LOW | c.804C>T|p.Leu268Leu |
S159 |
6 | BAA01g44130 | A01 | 29269868 | G | A | missense_variant | MODERATE | c.822G>A|p.Met274Ile |
S79 S91 |
7 | BAA01g44130 | A01 | 29269947 | C | T | missense_variant | MODERATE | c.901C>T|p.Pro301Ser |
S88 |
8 | BAA01g44130 | A01 | 29270001 | G | A | missense_variant | MODERATE | c.955G>A|p.Ala319Thr |
S104 |
9 | BAA01g44130 | A01 | 29270154 | C | T | missense_variant | MODERATE | c.1108C>T|p.Pro370Ser |
S168 |
10 | BAA01g44130 | A01 | 29272613 | C | T | missense_variant | MODERATE | c.2608C>T|p.Pro870Ser |
S41 |
11 | BAA01g44130 | A01 | 29272650 | G | A | missense_variant | MODERATE | c.2645G>A|p.Gly882Asp |
S293 |
12 | BAA01g44130 | A01 | 29273101 | C | T | downstream_gene_variant | MODIFIER | c.*285C>T| |
S165 |