Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01160 | A08 | 842572 | G | A | missense_variant | MODERATE | c.1778C>T|p.Thr593Met |
S269 |
2 | BAA08g01160 | A08 | 842817 | C | T | synonymous_variant | LOW | c.1533G>A|p.Ala511Ala |
S28 |
3 | BAA08g01160 | A08 | 843476 | G | A | missense_variant | MODERATE | c.874C>T|p.Pro292Ser |
S298 |
4 | BAA08g01160 | A08 | 845268 | G | A | upstream_gene_variant | MODIFIER | c.-919C>T| |
S194 |
5 | BAA08g01160 | A08 | 845497 | C | T | upstream_gene_variant | MODIFIER | c.-1148G>A| |
S179 |
6 | BAA08g01160 | A08 | 845550 | C | T | upstream_gene_variant | MODIFIER | c.-1201G>A| |
S235 |
7 | BAA08g01160 | A08 | 848501 | C | T | upstream_gene_variant | MODIFIER | c.-4152G>A| |
S66 |
8 | BAA08g01160 | A08 | 848843 | G | A | upstream_gene_variant | MODIFIER | c.-4494C>T| |
S35 |