Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44540 | A02 | 36678549 | G | A | downstream_gene_variant | MODIFIER | c.*1639C>T| |
S288 |
2 | BAA02g44540 | A02 | 36680414 | C | T | missense_variant | MODERATE | c.1666G>A|p.Glu556Lys |
S15 S153 S156 S213 S3 S34 S4 S6 |
3 | BAA02g44540 | A02 | 36680551 | G | A | missense_variant | MODERATE | c.1624C>T|p.Pro542Ser |
S148 S210 S31 |
4 | BAA02g44540 | A02 | 36681854 | G | A | synonymous_variant | LOW | c.1029C>T|p.Ala343Ala |
S298 |
5 | BAA02g44540 | A02 | 36681867 | G | A | missense_variant | MODERATE | c.1016C>T|p.Thr339Met |
S230 |
6 | BAA02g44540 | A02 | 36682721 | G | A | splice_region_variant&intron_variant | LOW | c.549-4C>T| |
S72 |
7 | BAA02g44540 | A02 | 36683662 | C | T | synonymous_variant | LOW | c.126G>A|p.Arg42Arg |
S64 |
8 | BAA02g44540 | A02 | 36684199 | C | T | upstream_gene_variant | MODIFIER | c.-412G>A| |
S283 |
9 | BAA02g44540 | A02 | 36684900 | G | A | upstream_gene_variant | MODIFIER | c.-1113C>T| |
S159 S187 S243 S298 |
10 | BAA02g44540 | A02 | 36685478 | G | A | upstream_gene_variant | MODIFIER | c.-1691C>T| |
S150 |
11 | BAA02g44540 | A02 | 36686534 | G | A | upstream_gene_variant | MODIFIER | c.-2747C>T| |
S139 |
12 | BAA02g44540 | A02 | 36688017 | G | A | upstream_gene_variant | MODIFIER | c.-4230C>T| |
S60 |