Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15050 | A01 | 7177456 | C | T | synonymous_variant | LOW | c.93C>T|p.Tyr31Tyr |
S167 |
2 | BAA01g15050 | A01 | 7177485 | C | T | missense_variant | MODERATE | c.122C>T|p.Thr41Ile |
S187 S188 S276 |
3 | BAA01g15050 | A01 | 7178138 | C | T | missense_variant | MODERATE | c.775C>T|p.Pro259Ser |
S108 |
4 | BAA01g15050 | A01 | 7178285 | G | A | splice_region_variant&intron_variant | LOW | c.818-4G>A| |
S296 |
5 | BAA01g15050 | A01 | 7178288 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.818-1G>A| |
S115 |