Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g09150 | A08 | 8346054 | C | T | upstream_gene_variant | MODIFIER | c.-4512C>T| |
S261 |
2 | BAA08g09150 | A08 | 8348774 | G | A | upstream_gene_variant | MODIFIER | c.-1792G>A| |
S115 |
3 | BAA08g09150 | A08 | 8348938 | G | A | upstream_gene_variant | MODIFIER | c.-1628G>A| |
S35 |
4 | BAA08g09150 | A08 | 8349545 | G | A | upstream_gene_variant | MODIFIER | c.-1021G>A| |
S20 |
5 | BAA08g09150 | A08 | 8349632 | T | A | upstream_gene_variant | MODIFIER | c.-934T>A| |
S182 |
6 | BAA08g09150 | A08 | 8350830 | G | A | missense_variant | MODERATE | c.265G>A|p.Glu89Lys |
S131 |
7 | BAA08g09150 | A08 | 8352406 | G | A | intron_variant | MODIFIER | c.920-19G>A| |
S108 |
8 | BAA08g09150 | A08 | 8352771 | C | T | intron_variant | MODIFIER | c.1085+85C>T| |
S278 |
9 | BAA08g09150 | A08 | 8353975 | G | A | intron_variant | MODIFIER | c.1085+1289G>A| |
S200 |
10 | BAA08g09150 | A08 | 8354381 | A | T | intron_variant | MODIFIER | c.1086-1531A>T| |
S250 |
11 | BAA08g09150 | A08 | 8355989 | G | A | missense_variant | MODERATE | c.1163G>A|p.Gly388Glu |
S202 |
12 | BAA08g09150 | A08 | 8360428 | C | T | downstream_gene_variant | MODIFIER | c.*4393C>T| |
S126 |