Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38820 | A02 | 33015033 | G | A | upstream_gene_variant | MODIFIER | c.-2893G>A| |
S164 |
2 | BAA02g38820 | A02 | 33015313 | C | T | upstream_gene_variant | MODIFIER | c.-2613C>T| |
S189 |
3 | BAA02g38820 | A02 | 33016401 | G | A | upstream_gene_variant | MODIFIER | c.-1525G>A| |
S166 |
4 | BAA02g38820 | A02 | 33016554 | G | A | upstream_gene_variant | MODIFIER | c.-1372G>A| |
S302 |
5 | BAA02g38820 | A02 | 33016698 | G | A | upstream_gene_variant | MODIFIER | c.-1228G>A| |
S293 |
6 | BAA02g38820 | A02 | 33017830 | C | T | upstream_gene_variant | MODIFIER | c.-96C>T| |
S18 |
7 | BAA02g38820 | A02 | 33017864 | C | T | upstream_gene_variant | MODIFIER | c.-62C>T| |
S139 |
8 | BAA02g38820 | A02 | 33017876 | C | T | upstream_gene_variant | MODIFIER | c.-50C>T| |
S193 |
9 | BAA02g38820 | A02 | 33018363 | C | T | synonymous_variant | LOW | c.438C>T|p.Tyr146Tyr |
S282 |
10 | BAA02g38820 | A02 | 33018493 | G | A | missense_variant | MODERATE | c.568G>A|p.Glu190Lys |
S148 S30 S31 |
11 | BAA02g38820 | A02 | 33018737 | C | T | missense_variant | MODERATE | c.812C>T|p.Ala271Val |
S263 |
12 | BAA02g38820 | A02 | 33019456 | C | T | downstream_gene_variant | MODIFIER | c.*199C>T| |
S211 |
13 | BAA02g38820 | A02 | 33019584 | G | A | downstream_gene_variant | MODIFIER | c.*327G>A| |
S153 S213 |
14 | BAA02g38820 | A02 | 33020940 | C | T | downstream_gene_variant | MODIFIER | c.*1683C>T| |
S180 |