Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27900 | A02 | 15716154 | C | T | downstream_gene_variant | MODIFIER | c.*2308G>A| |
S296 |
2 | BAA02g27900 | A02 | 15718556 | C | T | missense_variant | MODERATE | c.1355G>A|p.Arg452Lys |
S15 S2 S4 S6 |
3 | BAA02g27900 | A02 | 15718679 | G | A | missense_variant | MODERATE | c.1232C>T|p.Pro411Leu |
S231 |
4 | BAA02g27900 | A02 | 15718955 | C | T | missense_variant | MODERATE | c.956G>A|p.Gly319Asp |
S250 |
5 | BAA02g27900 | A02 | 15718972 | C | T | synonymous_variant | LOW | c.939G>A|p.Ala313Ala |
S183 S198 |
6 | BAA02g27900 | A02 | 15718974 | C | T | missense_variant | MODERATE | c.937G>A|p.Ala313Thr |
S179 |
7 | BAA02g27900 | A02 | 15719382 | C | T | missense_variant | MODERATE | c.529G>A|p.Val177Ile |
S283 |
8 | BAA02g27900 | A02 | 15720457 | C | T | upstream_gene_variant | MODIFIER | c.-547G>A| |
S183 S198 |
9 | BAA02g27900 | A02 | 15722596 | C | T | upstream_gene_variant | MODIFIER | c.-2686G>A| |
S105 S106 |
10 | BAA02g27900 | A02 | 15723538 | G | A | upstream_gene_variant | MODIFIER | c.-3628C>T| |
S144 |
11 | BAA02g27900 | A02 | 15723712 | G | A | upstream_gene_variant | MODIFIER | c.-3802C>T| |
S38 |
12 | BAA02g27900 | A02 | 15724317 | G | A | upstream_gene_variant | MODIFIER | c.-4407C>T| |
S133 |
13 | BAA02g27900 | A02 | 15724601 | C | T | upstream_gene_variant | MODIFIER | c.-4691G>A| |
S283 |