Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g43670 | A05 | 41021911 | C | T | downstream_gene_variant | MODIFIER | c.*3640G>A| |
S6 |
2 | BAA05g43670 | A05 | 41022318 | G | A | downstream_gene_variant | MODIFIER | c.*3233C>T| |
S150 |
3 | BAA05g43670 | A05 | 41022787 | G | A | downstream_gene_variant | MODIFIER | c.*2764C>T| |
S132 S137 S215 S89 |
4 | BAA05g43670 | A05 | 41025877 | G | A | missense_variant | MODERATE | c.1468C>T|p.Pro490Ser |
S79 S84 |
5 | BAA05g43670 | A05 | 41025916 | C | T | missense_variant | MODERATE | c.1429G>A|p.Glu477Lys |
S4 |
6 | BAA05g43670 | A05 | 41026079 | C | T | synonymous_variant | LOW | c.1266G>A|p.Arg422Arg |
S246 |
7 | BAA05g43670 | A05 | 41026347 | C | T | missense_variant | MODERATE | c.998G>A|p.Arg333Lys |
S65 |
8 | BAA05g43670 | A05 | 41026786 | G | A | synonymous_variant | LOW | c.559C>T|p.Leu187Leu |
S38 |
9 | BAA05g43670 | A05 | 41027880 | C | T | upstream_gene_variant | MODIFIER | c.-446G>A| |
S303 |
10 | BAA05g43670 | A05 | 41028484 | G | A | upstream_gene_variant | MODIFIER | c.-1050C>T| |
S219 S72 |
11 | BAA05g43670 | A05 | 41028920 | G | A | upstream_gene_variant | MODIFIER | c.-1486C>T| |
S224 |