Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01490 | A04 | 857171 | C | T | upstream_gene_variant | MODIFIER | c.-139C>T| |
S174 S241 S265 S27 |
2 | BAA04g01490 | A04 | 857361 | G | A | missense_variant | MODERATE | c.52G>A|p.Ala18Thr |
S61 |
3 | BAA04g01490 | A04 | 857715 | C | T | missense_variant | MODERATE | c.271C>T|p.Pro91Ser |
S82 S92 |
4 | BAA04g01490 | A04 | 858520 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.718-1G>A| |
S278 |
5 | BAA04g01490 | A04 | 858521 | G | A | missense_variant&splice_region_variant | MODERATE | c.718G>A|p.Ala240Thr |
S273 |