Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g37560 | A05 | 36979378 | C | T | missense_variant | MODERATE | c.784G>A|p.Ala262Thr |
S72 |
2 | BAA05g37560 | A05 | 36979491 | G | A | missense_variant | MODERATE | c.671C>T|p.Thr224Ile |
S88 |
3 | BAA05g37560 | A05 | 36982180 | G | A | upstream_gene_variant | MODIFIER | c.-1731C>T| |
S43 |
4 | BAA05g37560 | A05 | 36982680 | G | C | upstream_gene_variant | MODIFIER | c.-2231C>G| |
S154 S220 S257 S6 S92 |
5 | BAA05g37560 | A05 | 36983901 | C | T | upstream_gene_variant | MODIFIER | c.-3452G>A| |
S261 |
6 | BAA05g37560 | A05 | 36985006 | G | A | upstream_gene_variant | MODIFIER | c.-4557C>T| |
S265 |
7 | BAA05g37560 | A05 | 36985166 | G | A | upstream_gene_variant | MODIFIER | c.-4717C>T| |
S231 |