Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10910 | A02 | 4882241 | G | A | upstream_gene_variant | MODIFIER | c.-2733G>A| |
S282 |
2 | BAA02g10910 | A02 | 4884886 | G | A | upstream_gene_variant | MODIFIER | c.-88G>A| |
S163 |
3 | BAA02g10910 | A02 | 4885086 | C | T | missense_variant | MODERATE | c.113C>T|p.Ser38Phe |
S99 |
4 | BAA02g10910 | A02 | 4885214 | T | C | intron_variant | MODIFIER | c.201+40T>C| |
S289 S290 |
5 | BAA02g10910 | A02 | 4886086 | C | T | intron_variant | MODIFIER | c.202-686C>T| |
S117 |
6 | BAA02g10910 | A02 | 4886329 | C | T | intron_variant | MODIFIER | c.202-443C>T| |
S58 |
7 | BAA02g10910 | A02 | 4887258 | C | T | missense_variant | MODERATE | c.688C>T|p.Pro230Ser |
S99 |
8 | BAA02g10910 | A02 | 4888288 | G | A | missense_variant | MODERATE | c.1718G>A|p.Gly573Glu |
S289 S290 |
9 | BAA02g10910 | A02 | 4888326 | C | T | missense_variant | MODERATE | c.1756C>T|p.Pro586Ser |
S71 |