Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g53020 | A03 | 26004787 | G | A | missense_variant | MODERATE | c.1339C>T|p.Pro447Ser |
S5 |
2 | BAA03g53020 | A03 | 26004806 | C | T | synonymous_variant | LOW | c.1320G>A|p.Thr440Thr |
S2 |
3 | BAA03g53020 | A03 | 26004998 | T | G | synonymous_variant | LOW | c.1128A>C|p.Arg376Arg |
S258 |
4 | BAA03g53020 | A03 | 26005229 | C | T | synonymous_variant | LOW | c.897G>A|p.Gly299Gly |
S193 |
5 | BAA03g53020 | A03 | 26005915 | C | T | splice_region_variant&intron_variant | LOW | c.882+5G>A| |
S34 |
6 | BAA03g53020 | A03 | 26006006 | G | A | missense_variant | MODERATE | c.796C>T|p.Pro266Ser |
S64 |
7 | BAA03g53020 | A03 | 26006240 | C | T | missense_variant | MODERATE | c.562G>A|p.Val188Met |
S163 |
8 | BAA03g53020 | A03 | 26006451 | C | T | stop_gained | HIGH | c.351G>A|p.Trp117* |
S92 |
9 | BAA03g53020 | A03 | 26006497 | G | A | missense_variant | MODERATE | c.305C>T|p.Ala102Val |
S52 |
10 | BAA03g53020 | A03 | 26007140 | A | T | upstream_gene_variant | MODIFIER | c.-339T>A| |
S220 |
11 | BAA03g53020 | A03 | 26007743 | C | T | upstream_gene_variant | MODIFIER | c.-942G>A| |
S19 |
12 | BAA03g53020 | A03 | 26008777 | G | A | upstream_gene_variant | MODIFIER | c.-1976C>T| |
S135 |
13 | BAA03g53020 | A03 | 26009761 | G | A | upstream_gene_variant | MODIFIER | c.-2960C>T| |
S68 |
14 | BAA03g53020 | A03 | 26011728 | G | A | upstream_gene_variant | MODIFIER | c.-4927C>T| |
S164 |