Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05270 | A02 | 2304968 | G | A | missense_variant | MODERATE | c.1759C>T|p.His587Tyr |
S148 S210 S30 S31 |
2 | BAA02g05270 | A02 | 2305338 | G | A | missense_variant | MODERATE | c.1478C>T|p.Pro493Leu |
S23 |
3 | BAA02g05270 | A02 | 2305404 | G | A | missense_variant | MODERATE | c.1412C>T|p.Ala471Val |
S280 |
4 | BAA02g05270 | A02 | 2305500 | G | A | missense_variant | MODERATE | c.1316C>T|p.Pro439Leu |
S125 |
5 | BAA02g05270 | A02 | 2306255 | C | T | stop_gained | HIGH | c.1098G>A|p.Trp366* |
S277 S298 |
6 | BAA02g05270 | A02 | 2308501 | C | T | synonymous_variant | LOW | c.207G>A|p.Thr69Thr |
S42 |
7 | BAA02g05270 | A02 | 2308513 | A | G | synonymous_variant | LOW | c.195T>C|p.Ala65Ala |
S268 |
8 | BAA02g05270 | A02 | 2308844 | G | A | upstream_gene_variant | MODIFIER | c.-47C>T| |
S17 |
9 | BAA02g05270 | A02 | 2309111 | C | T | upstream_gene_variant | MODIFIER | c.-314G>A| |
S97 |
10 | BAA02g05270 | A02 | 2309885 | C | T | upstream_gene_variant | MODIFIER | c.-1088G>A| |
S65 |
11 | BAA02g05270 | A02 | 2311617 | C | A | upstream_gene_variant | MODIFIER | c.-2820G>T| |
S198 S213 |
12 | BAA02g05270 | A02 | 2312027 | G | A | upstream_gene_variant | MODIFIER | c.-3230C>T| |
S266 |
13 | BAA02g05270 | A02 | 2312780 | C | T | upstream_gene_variant | MODIFIER | c.-3983G>A| |
S28 |