Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20500 | A02 | 10878751 | G | A | downstream_gene_variant | MODIFIER | c.*2377C>T| |
S41 |
2 | BAA02g20500 | A02 | 10881323 | C | T | synonymous_variant | LOW | c.1353G>A|p.Ser451Ser |
S193 |
3 | BAA02g20500 | A02 | 10881356 | G | A | synonymous_variant | LOW | c.1320C>T|p.Phe440Phe |
S166 |
4 | BAA02g20500 | A02 | 10881683 | C | T | stop_gained | HIGH | c.993G>A|p.Trp331* |
S25 |
5 | BAA02g20500 | A02 | 10881823 | C | T | missense_variant | MODERATE | c.853G>A|p.Glu285Lys |
S249 |
6 | BAA02g20500 | A02 | 10882603 | G | A | missense_variant | MODERATE | c.73C>T|p.Leu25Phe |
S91 |
7 | BAA02g20500 | A02 | 10882636 | G | A | synonymous_variant | LOW | c.40C>T|p.Leu14Leu |
S200 |
8 | BAA02g20500 | A02 | 10883452 | G | A | upstream_gene_variant | MODIFIER | c.-777C>T| |
S69 |
9 | BAA02g20500 | A02 | 10884490 | C | T | upstream_gene_variant | MODIFIER | c.-1815G>A| |
S108 |
10 | BAA02g20500 | A02 | 10886611 | G | A | upstream_gene_variant | MODIFIER | c.-3936C>T| |
S155 S211 |
11 | BAA02g20500 | A02 | 10886648 | C | T | upstream_gene_variant | MODIFIER | c.-3973G>A| |
S40 S49 |
12 | BAA02g20500 | A02 | 10887190 | G | A | upstream_gene_variant | MODIFIER | c.-4515C>T| |
S210 |
13 | BAA02g20500 | A02 | 10887414 | G | A | upstream_gene_variant | MODIFIER | c.-4739C>T| |
S148 S30 S31 |