Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g09970 | A04 | 16195601 | C | T | upstream_gene_variant | MODIFIER | c.-4715C>T| |
S53 |
2 | BAA04g09970 | A04 | 16195620 | C | T | upstream_gene_variant | MODIFIER | c.-4696C>T| |
S284 |
3 | BAA04g09970 | A04 | 16195762 | G | A | upstream_gene_variant | MODIFIER | c.-4554G>A| |
S38 |
4 | BAA04g09970 | A04 | 16197448 | C | A | upstream_gene_variant | MODIFIER | c.-2868C>A| |
S148 S210 |
5 | BAA04g09970 | A04 | 16198733 | G | A | upstream_gene_variant | MODIFIER | c.-1583G>A| |
S40 S49 |
6 | BAA04g09970 | A04 | 16200253 | G | A | upstream_gene_variant | MODIFIER | c.-63G>A| |
S127 |
7 | BAA04g09970 | A04 | 16200570 | C | T | synonymous_variant | LOW | c.255C>T|p.Pro85Pro |
S286 |
8 | BAA04g09970 | A04 | 16200938 | C | T | missense_variant | MODERATE | c.464C>T|p.Ala155Val |
S247 |
9 | BAA04g09970 | A04 | 16201262 | C | T | missense_variant | MODERATE | c.640C>T|p.Pro214Ser |
S291 |