Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18130 | A01 | 8885057 | C | T | upstream_gene_variant | MODIFIER | c.-4825C>T| |
S128 |
2 | BAA01g18130 | A01 | 8889809 | C | T | upstream_gene_variant | MODIFIER | c.-73C>T| |
S247 |
3 | BAA01g18130 | A01 | 8890330 | G | A | synonymous_variant | LOW | c.351G>A|p.Gln117Gln |
S275 |
4 | BAA01g18130 | A01 | 8890866 | C | T | synonymous_variant | LOW | c.726C>T|p.His242His |
S62 |
5 | BAA01g18130 | A01 | 8891171 | G | A | missense_variant | MODERATE | c.1031G>A|p.Arg344His |
S138 |
6 | BAA01g18130 | A01 | 8892061 | G | A | missense_variant | MODERATE | c.1426G>A|p.Ala476Thr |
S72 S78 |
7 | BAA01g18130 | A01 | 8892217 | G | A | missense_variant | MODERATE | c.1582G>A|p.Ala528Thr |
S1 S90 |
8 | BAA01g18130 | A01 | 8893167 | C | T | synonymous_variant | LOW | c.1785C>T|p.Ser595Ser |
S82 S92 |
9 | BAA01g18130 | A01 | 8893285 | G | A | missense_variant | MODERATE | c.1903G>A|p.Glu635Lys |
S40 S49 |
10 | BAA01g18130 | A01 | 8895971 | G | A | downstream_gene_variant | MODIFIER | c.*2405G>A| |
S297 |
11 | BAA01g18130 | A01 | 8896383 | G | A | downstream_gene_variant | MODIFIER | c.*2817G>A| |
S262 |
12 | BAA01g18130 | A01 | 8897329 | G | A | downstream_gene_variant | MODIFIER | c.*3763G>A| |
S239 |
13 | BAA01g18130 | A01 | 8897626 | G | A | downstream_gene_variant | MODIFIER | c.*4060G>A| |
S14 S224 |
14 | BAA01g18130 | A01 | 8897974 | C | T | downstream_gene_variant | MODIFIER | c.*4408C>T| |
S247 |