Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g06670 | A07 | 16031021 | G | A | upstream_gene_variant | MODIFIER | c.-1124G>A| |
S146 |
2 | BAA07g06670 | A07 | 16032362 | G | A | missense_variant | MODERATE | c.143G>A|p.Arg48His |
S124 |
3 | BAA07g06670 | A07 | 16032557 | C | T | missense_variant | MODERATE | c.338C>T|p.Thr113Ile |
S195 |
4 | BAA07g06670 | A07 | 16032742 | C | T | missense_variant | MODERATE | c.523C>T|p.Leu175Phe |
S143 S56 |
5 | BAA07g06670 | A07 | 16034050 | C | T | synonymous_variant | LOW | c.1557C>T|p.Leu519Leu |
S165 |
6 | BAA07g06670 | A07 | 16034419 | G | A | missense_variant | MODERATE | c.1769G>A|p.Gly590Glu |
S122 |
7 | BAA07g06670 | A07 | 16034803 | C | T | missense_variant | MODERATE | c.2153C>T|p.Pro718Leu |
S266 |
8 | BAA07g06670 | A07 | 16035093 | G | A | synonymous_variant | LOW | c.2370G>A|p.Leu790Leu |
S292 |
9 | BAA07g06670 | A07 | 16035828 | C | T | synonymous_variant | LOW | c.2835C>T|p.Val945Val |
S133 |
10 | BAA07g06670 | A07 | 16036507 | G | A | downstream_gene_variant | MODIFIER | c.*472G>A| |
S62 |