Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20560 | A02 | 10909106 | C | T | upstream_gene_variant | MODIFIER | c.-364C>T| |
S152 |
2 | BAA02g20560 | A02 | 10909518 | C | T | missense_variant | MODERATE | c.49C>T|p.Pro17Ser |
S260 |
3 | BAA02g20560 | A02 | 10909561 | C | T | missense_variant | MODERATE | c.92C>T|p.Pro31Leu |
S189 |
4 | BAA02g20560 | A02 | 10910653 | C | T | stop_gained | HIGH | c.634C>T|p.Arg212* |
S80 |
5 | BAA02g20560 | A02 | 10911342 | C | T | stop_gained | HIGH | c.1057C>T|p.Gln353* |
S77 S82 |
6 | BAA02g20560 | A02 | 10911488 | G | A | missense_variant | MODERATE | c.1203G>A|p.Met401Ile |
S122 |
7 | BAA02g20560 | A02 | 10912064 | G | A | splice_region_variant&intron_variant | LOW | c.1458+6G>A| |
S43 |