Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g20950 | A08 | 16028349 | C | T | synonymous_variant | LOW | c.30C>T|p.Ala10Ala |
S169 S60 |
2 | BAA08g20950 | A08 | 16030288 | C | T | missense_variant | MODERATE | c.1469C>T|p.Ser490Phe |
S34 |
3 | BAA08g20950 | A08 | 16031120 | C | T | missense_variant | MODERATE | c.2108C>T|p.Ser703Phe |
S136 |
4 | BAA08g20950 | A08 | 16031392 | G | A | intron_variant | MODIFIER | c.2218-146G>A| |
S282 |
5 | BAA08g20950 | A08 | 16031645 | C | T | synonymous_variant | LOW | c.2325C>T|p.Ile775Ile |
S278 |
6 | BAA08g20950 | A08 | 16032645 | G | A | missense_variant | MODERATE | c.3325G>A|p.Val1109Ile |
S179 |
7 | BAA08g20950 | A08 | 16032895 | C | T | missense_variant | MODERATE | c.3575C>T|p.Ser1192Phe |
S13 S168 S219 |
8 | BAA08g20950 | A08 | 16034356 | C | T | missense_variant | MODERATE | c.5036C>T|p.Pro1679Leu |
S6 |
9 | BAA08g20950 | A08 | 16034385 | C | T | missense_variant | MODERATE | c.5065C>T|p.Pro1689Ser |
S173 |
10 | BAA08g20950 | A08 | 16035093 | C | T | missense_variant | MODERATE | c.5404C>T|p.Pro1802Ser |
S206 S26 |