Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29430 | A02 | 16841232 | G | A | splice_donor_variant&intron_variant | HIGH | c.181+1G>A| |
S229 |
2 | BAA02g29430 | A02 | 16841625 | G | A | missense_variant | MODERATE | c.412G>A|p.Ala138Thr |
S263 |
3 | BAA02g29430 | A02 | 16842509 | G | A | stop_gained | HIGH | c.885G>A|p.Trp295* |
S134 |
4 | BAA02g29430 | A02 | 16842531 | C | T | missense_variant | MODERATE | c.907C>T|p.Leu303Phe |
S185 |
5 | BAA02g29430 | A02 | 16843375 | G | A | missense_variant&splice_region_variant | MODERATE | c.1305G>A|p.Met435Ile |
S48 |
6 | BAA02g29430 | A02 | 16843503 | C | T | missense_variant | MODERATE | c.1433C>T|p.Pro478Leu |
S262 |
7 | BAA02g29430 | A02 | 16847010 | C | T | missense_variant | MODERATE | c.1810C>T|p.Pro604Ser |
S164 |
8 | BAA02g29430 | A02 | 16847139 | C | T | missense_variant | MODERATE | c.1939C>T|p.Arg647Cys |
S275 |
9 | BAA02g29430 | A02 | 16847140 | G | A | missense_variant | MODERATE | c.1940G>A|p.Arg647His |
S37 |
10 | BAA02g29430 | A02 | 16847308 | C | T | missense_variant | MODERATE | c.2108C>T|p.Ala703Val |
S6 |
11 | BAA02g29430 | A02 | 16848955 | G | A | missense_variant | MODERATE | c.3660G>A|p.Met1220Ile |
S158 |