Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g31590 | A01 | 20655740 | G | A | downstream_gene_variant | MODIFIER | c.*3296C>T| |
S75 |
2 | BAA01g31590 | A01 | 20656445 | C | G | downstream_gene_variant | MODIFIER | c.*2591G>C| |
S85 |
3 | BAA01g31590 | A01 | 20656880 | C | T | downstream_gene_variant | MODIFIER | c.*2156G>A| |
S277 |
4 | BAA01g31590 | A01 | 20656937 | C | T | downstream_gene_variant | MODIFIER | c.*2099G>A| |
S136 |
5 | BAA01g31590 | A01 | 20657412 | C | T | downstream_gene_variant | MODIFIER | c.*1624G>A| |
S269 |
6 | BAA01g31590 | A01 | 20657553 | G | A | downstream_gene_variant | MODIFIER | c.*1483C>T| |
S123 |
7 | BAA01g31590 | A01 | 20658776 | G | A | downstream_gene_variant | MODIFIER | c.*260C>T| |
S275 |
8 | BAA01g31590 | A01 | 20661205 | G | A | intron_variant | MODIFIER | c.580+348C>T| |
S280 |
9 | BAA01g31590 | A01 | 20661588 | C | T | missense_variant | MODERATE | c.545G>A|p.Arg182Lys |
S157 |
10 | BAA01g31590 | A01 | 20661590 | C | T | synonymous_variant | LOW | c.543G>A|p.Val181Val |
S69 |
11 | BAA01g31590 | A01 | 20661657 | G | A | missense_variant | MODERATE | c.476C>T|p.Ser159Phe |
S268 |
12 | BAA01g31590 | A01 | 20666652 | C | T | upstream_gene_variant | MODIFIER | c.-4520G>A| |
S14 |