Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35660 | A09 | 44039824 | C | T | upstream_gene_variant | MODIFIER | c.-4648C>T| |
S146 |
2 | BAA09g35660 | A09 | 44040681 | G | A | upstream_gene_variant | MODIFIER | c.-3791G>A| |
S291 |
3 | BAA09g35660 | A09 | 44044870 | C | T | missense_variant | MODERATE | c.97C>T|p.Arg33Cys |
S150 |
4 | BAA09g35660 | A09 | 44045394 | C | T | synonymous_variant | LOW | c.577C>T|p.Leu193Leu |
S295 |
5 | BAA09g35660 | A09 | 44045583 | C | T | stop_gained | HIGH | c.766C>T|p.Gln256* |
S92 |
6 | BAA09g35660 | A09 | 44045980 | G | A | synonymous_variant | LOW | c.1035G>A|p.Glu345Glu |
S79 S91 |
7 | BAA09g35660 | A09 | 44046121 | G | A | synonymous_variant | LOW | c.1176G>A|p.Lys392Lys |
S264 |
8 | BAA09g35660 | A09 | 44047388 | C | T | missense_variant | MODERATE | c.1780C>T|p.Arg594Cys |
S287 |
9 | BAA09g35660 | A09 | 44047719 | C | T | missense_variant | MODERATE | c.2111C>T|p.Pro704Leu |
S153 |
10 | BAA09g35660 | A09 | 44052839 | G | A | downstream_gene_variant | MODIFIER | c.*4936G>A| |
S1 S228 |