Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40190 | A02 | 33953119 | C | T | upstream_gene_variant | MODIFIER | c.-4411C>T| |
S198 |
2 | BAA02g40190 | A02 | 33954607 | G | A | upstream_gene_variant | MODIFIER | c.-2923G>A| |
S34 |
3 | BAA02g40190 | A02 | 33954721 | C | T | upstream_gene_variant | MODIFIER | c.-2809C>T| |
S301 S304 |
4 | BAA02g40190 | A02 | 33955199 | C | T | upstream_gene_variant | MODIFIER | c.-2331C>T| |
S33 |
5 | BAA02g40190 | A02 | 33955642 | G | A | upstream_gene_variant | MODIFIER | c.-1888G>A| |
S184 |
6 | BAA02g40190 | A02 | 33956969 | G | A | upstream_gene_variant | MODIFIER | c.-561G>A| |
S55 |
7 | BAA02g40190 | A02 | 33957437 | C | T | upstream_gene_variant | MODIFIER | c.-93C>T| |
S46 |
8 | BAA02g40190 | A02 | 33957546 | C | T | missense_variant | MODERATE | c.17C>T|p.Thr6Ile |
S51 |
9 | BAA02g40190 | A02 | 33957617 | G | A | missense_variant | MODERATE | c.88G>A|p.Ala30Thr |
S44 |
10 | BAA02g40190 | A02 | 33957626 | G | A | missense_variant | MODERATE | c.97G>A|p.Val33Met |
S176 |
11 | BAA02g40190 | A02 | 33957813 | C | T | intron_variant | MODIFIER | c.114+170C>T| |
S205 |
12 | BAA02g40190 | A02 | 33959783 | G | A | downstream_gene_variant | MODIFIER | c.*1277G>A| |
S8 |
13 | BAA02g40190 | A02 | 33960057 | G | A | downstream_gene_variant | MODIFIER | c.*1551G>A| |
S174 S216 S27 |
14 | BAA02g40190 | A02 | 33961583 | C | T | downstream_gene_variant | MODIFIER | c.*3077C>T| |
S135 |