Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g18190 | A03 | 8008167 | C | T | missense_variant | MODERATE | c.401C>T|p.Pro134Leu |
S19 |
2 | BAA03g18190 | A03 | 8008368 | G | A | intron_variant | MODIFIER | c.427+175G>A| |
S216 S241 S27 S39 |
3 | BAA03g18190 | A03 | 8008585 | C | T | intron_variant | MODIFIER | c.427+392C>T| |
S113 |
4 | BAA03g18190 | A03 | 8009734 | C | T | splice_region_variant&synonymous_variant | LOW | c.828C>T|p.Pro276Pro |
S240 |