Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g25050 | A04 | 26346084 | G | A | intron_variant | MODIFIER | c.250+30G>A| |
S60 |
2 | BAA04g25050 | A04 | 26346439 | G | A | intron_variant | MODIFIER | c.250+385G>A| |
S194 |
3 | BAA04g25050 | A04 | 26346761 | G | A | intron_variant | MODIFIER | c.250+707G>A| |
S66 |
4 | BAA04g25050 | A04 | 26346833 | C | T | intron_variant | MODIFIER | c.250+779C>T| |
S59 |
5 | BAA04g25050 | A04 | 26346835 | C | T | intron_variant | MODIFIER | c.250+781C>T| |
S45 |
6 | BAA04g25050 | A04 | 26346894 | G | A | intron_variant | MODIFIER | c.251-742G>A| |
S293 |
7 | BAA04g25050 | A04 | 26347142 | G | A | intron_variant | MODIFIER | c.251-494G>A| |
S146 |
8 | BAA04g25050 | A04 | 26347589 | C | T | intron_variant | MODIFIER | c.251-47C>T| |
S284 |
9 | BAA04g25050 | A04 | 26348295 | C | T | missense_variant | MODERATE | c.722C>T|p.Thr241Ile |
S140 |
10 | BAA04g25050 | A04 | 26349226 | G | A | missense_variant | MODERATE | c.925G>A|p.Glu309Lys |
S233 |
11 | BAA04g25050 | A04 | 26349572 | C | T | downstream_gene_variant | MODIFIER | c.*248C>T| |
S80 |
12 | BAA04g25050 | A04 | 26349703 | G | A | downstream_gene_variant | MODIFIER | c.*379G>A| |
S165 |