Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g33660 | A08 | 21859665 | C | T | missense_variant | MODERATE | c.479C>T|p.Ser160Phe |
S286 |
2 | BAA08g33660 | A08 | 21860109 | G | A | intron_variant | MODIFIER | c.784-33G>A| |
S124 |
3 | BAA08g33660 | A08 | 21860760 | G | A | missense_variant | MODERATE | c.1136G>A|p.Gly379Glu |
S38 |
4 | BAA08g33660 | A08 | 21861164 | C | T | missense_variant | MODERATE | c.1391C>T|p.Thr464Ile |
S117 |
5 | BAA08g33660 | A08 | 21862211 | G | A | missense_variant | MODERATE | c.2024G>A|p.Gly675Glu |
S221 |
6 | BAA08g33660 | A08 | 21862947 | G | A | missense_variant | MODERATE | c.2611G>A|p.Glu871Lys |
S136 |