Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11400 | A09 | 6392624 | G | A | missense_variant | MODERATE | c.449G>A|p.Gly150Asp |
S117 |
2 | BAA09g11400 | A09 | 6392964 | C | T | missense_variant | MODERATE | c.572C>T|p.Ser191Phe |
S193 |
3 | BAA09g11400 | A09 | 6392976 | C | T | missense_variant | MODERATE | c.584C>T|p.Ser195Leu |
S76 |
4 | BAA09g11400 | A09 | 6393909 | G | A | synonymous_variant | LOW | c.936G>A|p.Ser312Ser |
S289 S290 |
5 | BAA09g11400 | A09 | 6394163 | C | T | missense_variant | MODERATE | c.1021C>T|p.Pro341Ser |
S54 |
6 | BAA09g11400 | A09 | 6394724 | C | T | missense_variant | MODERATE | c.1321C>T|p.Leu441Phe |
S217 S248 |
7 | BAA09g11400 | A09 | 6394772 | C | T | missense_variant | MODERATE | c.1369C>T|p.Leu457Phe |
S168 |
8 | BAA09g11400 | A09 | 6396616 | G | A | splice_region_variant&intron_variant | LOW | c.2077-5G>A| |
S174 S27 S39 |