Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g32980 | A02 | 28243007 | G | C | upstream_gene_variant | MODIFIER | c.-185G>C| |
S69 |
2 | BAA02g32980 | A02 | 28243992 | C | T | missense_variant | MODERATE | c.545C>T|p.Pro182Leu |
S273 |
3 | BAA02g32980 | A02 | 28244183 | C | T | missense_variant | MODERATE | c.665C>T|p.Pro222Leu |
S261 |
4 | BAA02g32980 | A02 | 28244277 | C | T | splice_region_variant&intron_variant | LOW | c.686-3C>T| |
S53 |
5 | BAA02g32980 | A02 | 28244441 | G | A | splice_region_variant&intron_variant | LOW | c.840+7G>A| |
S127 |
6 | BAA02g32980 | A02 | 28244942 | G | A | synonymous_variant | LOW | c.1092G>A|p.Lys364Lys |
S278 |
7 | BAA02g32980 | A02 | 28245775 | G | A | missense_variant | MODERATE | c.1501G>A|p.Glu501Lys |
S34 |
8 | BAA02g32980 | A02 | 28246008 | C | T | missense_variant | MODERATE | c.1655C>T|p.Ser552Phe |
S33 |
9 | BAA02g32980 | A02 | 28246358 | C | T | downstream_gene_variant | MODIFIER | c.*307C>T| |
S203 |
10 | BAA02g32980 | A02 | 28247241 | C | T | downstream_gene_variant | MODIFIER | c.*1190C>T| |
S239 |