Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29580 | A02 | 16928515 | G | A | upstream_gene_variant | MODIFIER | c.-3217G>A| |
S298 |
2 | BAA02g29580 | A02 | 16928864 | C | T | upstream_gene_variant | MODIFIER | c.-2868C>T| |
S171 |
3 | BAA02g29580 | A02 | 16930461 | G | A | upstream_gene_variant | MODIFIER | c.-1271G>A| |
S251 |
4 | BAA02g29580 | A02 | 16932806 | G | A | missense_variant | MODERATE | c.670G>A|p.Val224Met |
S225 S73 |
5 | BAA02g29580 | A02 | 16933120 | G | A | intron_variant | MODIFIER | c.882+24G>A| |
S149 |
6 | BAA02g29580 | A02 | 16933226 | C | T | synonymous_variant | LOW | c.894C>T|p.Val298Val |
S286 |
7 | BAA02g29580 | A02 | 16933283 | G | A | synonymous_variant | LOW | c.951G>A|p.Lys317Lys |
S280 |
8 | BAA02g29580 | A02 | 16933374 | G | A | missense_variant | MODERATE | c.1042G>A|p.Glu348Lys |
S229 |
9 | BAA02g29580 | A02 | 16933635 | C | T | intron_variant | MODIFIER | c.1110-13C>T| |
S224 |
10 | BAA02g29580 | A02 | 16933757 | G | A | missense_variant | MODERATE | c.1219G>A|p.Ala407Thr |
S240 |
11 | BAA02g29580 | A02 | 16933833 | C | T | missense_variant | MODERATE | c.1295C>T|p.Ser432Leu |
S87 |
12 | BAA02g29580 | A02 | 16934117 | C | T | downstream_gene_variant | MODIFIER | c.*178C>T| |
S112 |
13 | BAA02g29580 | A02 | 16934570 | G | A | downstream_gene_variant | MODIFIER | c.*631G>A| |
S111 |
14 | BAA02g29580 | A02 | 16934756 | G | A | downstream_gene_variant | MODIFIER | c.*817G>A| |
S48 |
15 | BAA02g29580 | A02 | 16938447 | G | A | downstream_gene_variant | MODIFIER | c.*4508G>A| |
S187 |