Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30340 | A02 | 17621338 | C | T | downstream_gene_variant | MODIFIER | c.*3398G>A| |
S299 |
2 | BAA02g30340 | A02 | 17623415 | C | T | downstream_gene_variant | MODIFIER | c.*1321G>A| |
S234 |
3 | BAA02g30340 | A02 | 17623961 | C | T | downstream_gene_variant | MODIFIER | c.*775G>A| |
S226 |
4 | BAA02g30340 | A02 | 17624560 | G | A | downstream_gene_variant | MODIFIER | c.*176C>T| |
S278 |
5 | BAA02g30340 | A02 | 17625139 | G | A | synonymous_variant | LOW | c.1911C>T|p.Thr637Thr |
S236 |
6 | BAA02g30340 | A02 | 17625357 | G | A | missense_variant | MODERATE | c.1693C>T|p.Pro565Ser |
S251 |
7 | BAA02g30340 | A02 | 17626680 | C | T | missense_variant | MODERATE | c.614G>A|p.Gly205Glu |
S305 |
8 | BAA02g30340 | A02 | 17626722 | G | A | missense_variant | MODERATE | c.572C>T|p.Pro191Leu |
S171 |
9 | BAA02g30340 | A02 | 17626845 | G | A | missense_variant | MODERATE | c.449C>T|p.Pro150Leu |
S7 |
10 | BAA02g30340 | A02 | 17626885 | G | A | missense_variant | MODERATE | c.409C>T|p.Leu137Phe |
S19 |
11 | BAA02g30340 | A02 | 17627591 | G | A | upstream_gene_variant | MODIFIER | c.-298C>T| |
S272 |
12 | BAA02g30340 | A02 | 17628228 | C | T | upstream_gene_variant | MODIFIER | c.-935G>A| |
S136 |
13 | BAA02g30340 | A02 | 17629130 | T | C | upstream_gene_variant | MODIFIER | c.-1837A>G| |
S272 |
14 | BAA02g30340 | A02 | 17629839 | G | A | upstream_gene_variant | MODIFIER | c.-2546C>T| |
S129 |
15 | BAA02g30340 | A02 | 17630056 | G | A | upstream_gene_variant | MODIFIER | c.-2763C>T| |
S67 |
16 | BAA02g30340 | A02 | 17630395 | G | A | upstream_gene_variant | MODIFIER | c.-3102C>T| |
S263 |