Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01800 | A09 | 1242352 | G | A | upstream_gene_variant | MODIFIER | c.-960G>A| |
S73 |
2 | BAA09g01800 | A09 | 1242420 | C | T | upstream_gene_variant | MODIFIER | c.-892C>T| |
S242 |
3 | BAA09g01800 | A09 | 1242968 | C | T | upstream_gene_variant | MODIFIER | c.-344C>T| |
S161 |
4 | BAA09g01800 | A09 | 1244021 | G | A | intron_variant | MODIFIER | c.26-490G>A| |
S229 |
5 | BAA09g01800 | A09 | 1244489 | G | A | intron_variant | MODIFIER | c.26-22G>A| |
S263 |
6 | BAA09g01800 | A09 | 1248033 | G | A | missense_variant | MODERATE | c.1814G>A|p.Gly605Asp |
S23 |
7 | BAA09g01800 | A09 | 1248503 | C | T | missense_variant | MODERATE | c.2059C>T|p.Leu687Phe |
S278 |
8 | BAA09g01800 | A09 | 1248594 | C | T | missense_variant | MODERATE | c.2150C>T|p.Ala717Val |
S217 S248 |
9 | BAA09g01800 | A09 | 1248699 | C | T | missense_variant | MODERATE | c.2255C>T|p.Pro752Leu |
S297 |
10 | BAA09g01800 | A09 | 1248702 | G | A | missense_variant | MODERATE | c.2258G>A|p.Gly753Glu |
S232 |
11 | BAA09g01800 | A09 | 1251718 | C | T | downstream_gene_variant | MODIFIER | c.*2376C>T| |
S64 |