Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g20070 | A05 | 12218647 | G | A | missense_variant | MODERATE | c.619G>A|p.Glu207Lys |
S104 S52 |
2 | BAA05g20070 | A05 | 12219188 | G | A | missense_variant&splice_region_variant | MODERATE | c.715G>A|p.Glu239Lys |
S297 |
3 | BAA05g20070 | A05 | 12220102 | G | A | stop_gained | HIGH | c.864G>A|p.Trp288* |
S122 |
4 | BAA05g20070 | A05 | 12220272 | C | T | missense_variant | MODERATE | c.1034C>T|p.Ala345Val |
S164 |
5 | BAA05g20070 | A05 | 12220411 | G | A | synonymous_variant | LOW | c.1173G>A|p.Pro391Pro |
S219 S72 |
6 | BAA05g20070 | A05 | 12220513 | G | T | synonymous_variant | LOW | c.1275G>T|p.Val425Val |
S173 |
7 | BAA05g20070 | A05 | 12220529 | G | A | missense_variant | MODERATE | c.1291G>A|p.Val431Ile |
S303 |
8 | BAA05g20070 | A05 | 12221225 | G | A | missense_variant | MODERATE | c.1912G>A|p.Glu638Lys |
S149 |
9 | BAA05g20070 | A05 | 12221406 | C | T | missense_variant | MODERATE | c.2093C>T|p.Thr698Met |
S201 |
10 | BAA05g20070 | A05 | 12221648 | G | A | missense_variant | MODERATE | c.2335G>A|p.Glu779Lys |
S124 |