Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g50660 | A03 | 24533756 | C | T | synonymous_variant | LOW | c.670C>T|p.Leu224Leu |
S199 |
2 | BAA03g50660 | A03 | 24534604 | C | T | synonymous_variant | LOW | c.1434C>T|p.Asp478Asp |
S90 |
3 | BAA03g50660 | A03 | 24534953 | C | T | stop_gained | HIGH | c.1783C>T|p.Gln595* |
S126 |
4 | BAA03g50660 | A03 | 24535029 | C | T | missense_variant | MODERATE | c.1859C>T|p.Ser620Leu |
S100 |
5 | BAA03g50660 | A03 | 24536229 | G | A | missense_variant | MODERATE | c.2890G>A|p.Gly964Arg |
S272 |
6 | BAA03g50660 | A03 | 24536288 | G | A | synonymous_variant | LOW | c.2949G>A|p.Leu983Leu |
S302 |
7 | BAA03g50660 | A03 | 24536822 | C | T | synonymous_variant | LOW | c.3360C>T|p.His1120His |
S140 |
8 | BAA03g50660 | A03 | 24537197 | G | A | missense_variant | MODERATE | c.3515G>A|p.Gly1172Glu |
S138 |
9 | BAA03g50660 | A03 | 24539168 | C | T | downstream_gene_variant | MODIFIER | c.*1856C>T| |
S82 S86 |
10 | BAA03g50660 | A03 | 24539173 | C | T | downstream_gene_variant | MODIFIER | c.*1861C>T| |
S184 S57 |
11 | BAA03g50660 | A03 | 24539576 | C | T | downstream_gene_variant | MODIFIER | c.*2264C>T| |
S301 S304 |
12 | BAA03g50660 | A03 | 24539650 | C | T | downstream_gene_variant | MODIFIER | c.*2338C>T| |
S184 |
13 | BAA03g50660 | A03 | 24540582 | T | A | downstream_gene_variant | MODIFIER | c.*3270T>A| |
S192 |