Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g20930 | A08 | 16019032 | G | A | synonymous_variant | LOW | c.180G>A|p.Lys60Lys |
S193 |
2 | BAA08g20930 | A08 | 16019332 | C | T | missense_variant | MODERATE | c.301C>T|p.Leu101Phe |
S138 |
3 | BAA08g20930 | A08 | 16020331 | G | A | missense_variant | MODERATE | c.862G>A|p.Gly288Arg |
S259 |
4 | BAA08g20930 | A08 | 16020874 | C | T | missense_variant | MODERATE | c.1154C>T|p.Pro385Leu |
S43 |
5 | BAA08g20930 | A08 | 16020894 | G | A | missense_variant | MODERATE | c.1174G>A|p.Asp392Asn |
S97 |
6 | BAA08g20930 | A08 | 16022330 | G | A | missense_variant | MODERATE | c.1921G>A|p.Asp641Asn |
S140 |
7 | BAA08g20930 | A08 | 16022593 | C | T | synonymous_variant | LOW | c.2184C>T|p.Phe728Phe |
S235 |
8 | BAA08g20930 | A08 | 16022623 | G | A | synonymous_variant | LOW | c.2214G>A|p.Leu738Leu |
S40 S49 |
9 | BAA08g20930 | A08 | 16022630 | G | A | missense_variant | MODERATE | c.2221G>A|p.Glu741Lys |
S297 |
10 | BAA08g20930 | A08 | 16023018 | C | T | synonymous_variant | LOW | c.2437C>T|p.Leu813Leu |
S119 |