Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65870 | A09 | 60460430 | G | A | missense_variant | MODERATE | c.1391C>T|p.Ala464Val |
S190 |
2 | BAA09g65870 | A09 | 60462244 | G | A | missense_variant | MODERATE | c.361C>T|p.Leu121Phe |
S96 |
3 | BAA09g65870 | A09 | 60462381 | G | A | missense_variant | MODERATE | c.224C>T|p.Thr75Ile |
S11 |
4 | BAA09g65870 | A09 | 60462416 | G | A | synonymous_variant | LOW | c.189C>T|p.Leu63Leu |
S262 |
5 | BAA09g65870 | A09 | 60462565 | G | A | missense_variant | MODERATE | c.40C>T|p.Leu14Phe |
S23 |
6 | BAA09g65870 | A09 | 60466275 | G | A | upstream_gene_variant | MODIFIER | c.-3671C>T| |
S281 |
7 | BAA09g65870 | A09 | 60467148 | C | T | upstream_gene_variant | MODIFIER | c.-4544G>A| |
S293 |