Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g01960 | A05 | 1064501 | C | T | downstream_gene_variant | MODIFIER | c.*1840G>A| |
S172 |
2 | BAA05g01960 | A05 | 1065107 | G | A | downstream_gene_variant | MODIFIER | c.*1234C>T| |
S112 |
3 | BAA05g01960 | A05 | 1067110 | G | A | missense_variant | MODERATE | c.1166C>T|p.Thr389Ile |
S16 |
4 | BAA05g01960 | A05 | 1067819 | C | T | intron_variant | MODIFIER | c.811-160G>A| |
S92 |
5 | BAA05g01960 | A05 | 1067869 | C | T | intron_variant | MODIFIER | c.810+146G>A| |
S38 |
6 | BAA05g01960 | A05 | 1068156 | C | T | intron_variant | MODIFIER | c.741+15G>A| |
S243 S299 |
7 | BAA05g01960 | A05 | 1068272 | C | T | missense_variant | MODERATE | c.640G>A|p.Ala214Thr |
S25 |
8 | BAA05g01960 | A05 | 1068644 | G | A | missense_variant | MODERATE | c.443C>T|p.Ser148Phe |
S217 S248 |
9 | BAA05g01960 | A05 | 1070755 | C | T | upstream_gene_variant | MODIFIER | c.-1196G>A| |
S60 |