Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17610 | A09 | 10559931 | G | A | missense_variant | MODERATE | c.113G>A|p.Arg38Lys |
S63 |
2 | BAA09g17610 | A09 | 10560981 | G | A | missense_variant | MODERATE | c.610G>A|p.Val204Ile |
S229 |
3 | BAA09g17610 | A09 | 10561222 | C | T | missense_variant | MODERATE | c.776C>T|p.Ser259Phe |
S5 |
4 | BAA09g17610 | A09 | 10562017 | C | T | missense_variant | MODERATE | c.1270C>T|p.Pro424Ser |
S116 |
5 | BAA09g17610 | A09 | 10562629 | C | T | splice_region_variant&intron_variant | LOW | c.1575+6C>T| |
S36 |
6 | BAA09g17610 | A09 | 10563779 | G | A | synonymous_variant | LOW | c.2109G>A|p.Leu703Leu |
S291 |
7 | BAA09g17610 | A09 | 10564230 | G | A | missense_variant | MODERATE | c.2314G>A|p.Gly772Ser |
S192 |
8 | BAA09g17610 | A09 | 10564424 | G | A | missense_variant | MODERATE | c.2427G>A|p.Met809Ile |
S259 |