Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21280 | A02 | 11411100 | C | T | upstream_gene_variant | MODIFIER | c.-2797C>T| |
S181 |
2 | BAA02g21280 | A02 | 11411125 | C | T | upstream_gene_variant | MODIFIER | c.-2772C>T| |
S53 |
3 | BAA02g21280 | A02 | 11414405 | C | T | missense_variant | MODERATE | c.509C>T|p.Thr170Met |
S6 |
4 | BAA02g21280 | A02 | 11415004 | G | A | synonymous_variant | LOW | c.639G>A|p.Gly213Gly |
S272 |
5 | BAA02g21280 | A02 | 11415129 | G | A | missense_variant | MODERATE | c.764G>A|p.Gly255Glu |
S111 |
6 | BAA02g21280 | A02 | 11415267 | G | A | missense_variant | MODERATE | c.902G>A|p.Gly301Glu |
S5 |
7 | BAA02g21280 | A02 | 11416033 | C | T | downstream_gene_variant | MODIFIER | c.*399C>T| |
S218 |
8 | BAA02g21280 | A02 | 11416237 | C | T | downstream_gene_variant | MODIFIER | c.*603C>T| |
S80 |
9 | BAA02g21280 | A02 | 11416395 | C | T | downstream_gene_variant | MODIFIER | c.*761C>T| |
S178 |
10 | BAA02g21280 | A02 | 11416474 | G | A | downstream_gene_variant | MODIFIER | c.*840G>A| |
S59 |