Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g34880 | A01 | 23315877 | G | A | missense_variant | MODERATE | c.170G>A|p.Arg57His |
S129 |
2 | BAA01g34880 | A01 | 23315917 | C | T | synonymous_variant | LOW | c.210C>T|p.Arg70Arg |
S149 |
3 | BAA01g34880 | A01 | 23315949 | C | T | missense_variant | MODERATE | c.242C>T|p.Thr81Met |
S134 S179 S193 |
4 | BAA01g34880 | A01 | 23316873 | C | T | missense_variant | MODERATE | c.766C>T|p.Pro256Ser |
S18 |
5 | BAA01g34880 | A01 | 23317718 | C | T | missense_variant | MODERATE | c.1093C>T|p.Pro365Ser |
S298 |
6 | BAA01g34880 | A01 | 23317964 | C | T | missense_variant | MODERATE | c.1339C>T|p.Pro447Ser |
S28 |
7 | BAA01g34880 | A01 | 23318324 | C | T | missense_variant | MODERATE | c.1699C>T|p.Pro567Ser |
S81 S85 |
8 | BAA01g34880 | A01 | 23318423 | C | T | missense_variant | MODERATE | c.1798C>T|p.Pro600Ser |
S115 |