Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g47860 | A03 | 22970189 | G | A | upstream_gene_variant | MODIFIER | c.-4711G>A| |
S171 |
2 | BAA03g47860 | A03 | 22970784 | C | T | upstream_gene_variant | MODIFIER | c.-4116C>T| |
S293 |
3 | BAA03g47860 | A03 | 22974959 | C | T | synonymous_variant | LOW | c.60C>T|p.Arg20Arg |
S116 |
4 | BAA03g47860 | A03 | 22975022 | G | A | stop_gained | HIGH | c.123G>A|p.Trp41* |
S298 |
5 | BAA03g47860 | A03 | 22977413 | G | A | missense_variant | MODERATE | c.1654G>A|p.Glu552Lys |
S7 |
6 | BAA03g47860 | A03 | 22977499 | G | A | stop_gained | HIGH | c.1740G>A|p.Trp580* |
S85 |
7 | BAA03g47860 | A03 | 22978077 | G | A | missense_variant | MODERATE | c.2086G>A|p.Val696Ile |
S15 S153 S156 S2 S213 S3 S34 S4 S6 |
8 | BAA03g47860 | A03 | 22979522 | C | T | synonymous_variant | LOW | c.2328C>T|p.Pro776Pro |
S266 |
9 | BAA03g47860 | A03 | 22980855 | G | A | synonymous_variant | LOW | c.3264G>A|p.Thr1088Thr |
S171 S233 |
10 | BAA03g47860 | A03 | 22981555 | C | T | missense_variant | MODERATE | c.3797C>T|p.Ser1266Leu |
S120 |
11 | BAA03g47860 | A03 | 22981906 | C | T | missense_variant | MODERATE | c.4055C>T|p.Pro1352Leu |
S18 |
12 | BAA03g47860 | A03 | 22982487 | C | T | downstream_gene_variant | MODIFIER | c.*520C>T| |
S193 |
13 | BAA03g47860 | A03 | 22982549 | C | T | downstream_gene_variant | MODIFIER | c.*582C>T| |
S157 S163 |
14 | BAA03g47860 | A03 | 22983068 | C | T | downstream_gene_variant | MODIFIER | c.*1101C>T| |
S180 |