Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27510 | A01 | 15948652 | C | T | missense_variant | MODERATE | c.2128G>A|p.Ala710Thr |
S128 |
2 | BAA01g27510 | A01 | 15949550 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1540-1G>A| |
S295 |
3 | BAA01g27510 | A01 | 15951516 | C | T | missense_variant | MODERATE | c.259G>A|p.Val87Met |
S230 |
4 | BAA01g27510 | A01 | 15951671 | G | A | synonymous_variant | LOW | c.195C>T|p.Leu65Leu |
S37 |
5 | BAA01g27510 | A01 | 15951706 | C | T | missense_variant | MODERATE | c.160G>A|p.Glu54Lys |
S159 S234 |
6 | BAA01g27510 | A01 | 15952516 | G | A | intron_variant | MODIFIER | c.92-742C>T| |
S56 |
7 | BAA01g27510 | A01 | 15953965 | G | A | missense_variant | MODERATE | c.4C>T|p.Pro2Ser |
S294 |
8 | BAA01g27510 | A01 | 15954986 | C | T | upstream_gene_variant | MODIFIER | c.-1018G>A| |
S206 |
9 | BAA01g27510 | A01 | 15955048 | C | T | upstream_gene_variant | MODIFIER | c.-1080G>A| |
S282 |
10 | BAA01g27510 | A01 | 15956643 | C | T | upstream_gene_variant | MODIFIER | c.-2675G>A| |
S125 |
11 | BAA01g27510 | A01 | 15957654 | G | A | upstream_gene_variant | MODIFIER | c.-3686C>T| |
S122 S60 |
12 | BAA01g27510 | A01 | 15958280 | G | A | upstream_gene_variant | MODIFIER | c.-4312C>T| |
S236 S260 |
13 | BAA01g27510 | A01 | 15958936 | C | T | upstream_gene_variant | MODIFIER | c.-4968G>A| |
S39 |