Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22120 | A08 | 16703284 | C | T | synonymous_variant | LOW | c.528C>T|p.His176His |
S305 |
2 | BAA08g22120 | A08 | 16704045 | C | T | missense_variant | MODERATE | c.1289C>T|p.Ala430Val |
S138 |
3 | BAA08g22120 | A08 | 16704074 | C | T | splice_region_variant&intron_variant | LOW | c.1311+7C>T| |
S166 |
4 | BAA08g22120 | A08 | 16704152 | G | A | missense_variant | MODERATE | c.1321G>A|p.Val441Ile |
S165 S211 S227 |
5 | BAA08g22120 | A08 | 16704236 | G | A | missense_variant | MODERATE | c.1405G>A|p.Val469Ile |
S111 |
6 | BAA08g22120 | A08 | 16704883 | G | A | stop_gained | HIGH | c.2052G>A|p.Trp684* |
S190 |
7 | BAA08g22120 | A08 | 16704911 | G | A | missense_variant | MODERATE | c.2080G>A|p.Val694Ile |
S204 |
8 | BAA08g22120 | A08 | 16707085 | G | A | intron_variant | MODIFIER | c.2236+2018G>A| |
S195 |
9 | BAA08g22120 | A08 | 16711113 | C | T | missense_variant | MODERATE | c.2930C>T|p.Ala977Val |
S44 |