Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25460 | A02 | 13963504 | C | T | upstream_gene_variant | MODIFIER | c.-3880C>T| |
S157 S163 |
2 | BAA02g25460 | A02 | 13964745 | G | A | upstream_gene_variant | MODIFIER | c.-2639G>A| |
S5 |
3 | BAA02g25460 | A02 | 13966500 | C | T | upstream_gene_variant | MODIFIER | c.-884C>T| |
S270 |
4 | BAA02g25460 | A02 | 13967432 | G | A | missense_variant | MODERATE | c.49G>A|p.Glu17Lys |
S111 |
5 | BAA02g25460 | A02 | 13967504 | C | T | missense_variant | MODERATE | c.121C>T|p.Arg41Cys |
S71 |
6 | BAA02g25460 | A02 | 13968799 | C | T | missense_variant | MODERATE | c.731C>T|p.Pro244Leu |
S296 |
7 | BAA02g25460 | A02 | 13968956 | G | A | missense_variant | MODERATE | c.805G>A|p.Gly269Arg |
S153 S213 |
8 | BAA02g25460 | A02 | 13969294 | G | A | missense_variant | MODERATE | c.1061G>A|p.Gly354Glu |
S67 |
9 | BAA02g25460 | A02 | 13969366 | G | A | stop_gained | HIGH | c.1133G>A|p.Trp378* |
S34 |
10 | BAA02g25460 | A02 | 13972780 | C | T | downstream_gene_variant | MODIFIER | c.*3383C>T| |
S130 |