Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20230 | A10 | 18286042 | G | A | stop_gained | HIGH | c.57G>A|p.Trp19* |
S35 |
2 | BAA10g20230 | A10 | 18286853 | G | A | synonymous_variant | LOW | c.789G>A|p.Leu263Leu |
S80 |
3 | BAA10g20230 | A10 | 18286897 | G | A | missense_variant | MODERATE | c.833G>A|p.Gly278Glu |
S208 S219 |
4 | BAA10g20230 | A10 | 18287645 | G | A | synonymous_variant | LOW | c.1581G>A|p.Lys527Lys |
S28 |
5 | BAA10g20230 | A10 | 18288683 | G | A | missense_variant | MODERATE | c.2041G>A|p.Glu681Lys |
S112 |
6 | BAA10g20230 | A10 | 18289304 | G | A | missense_variant | MODERATE | c.2662G>A|p.Gly888Arg |
S217 S248 |
7 | BAA10g20230 | A10 | 18289441 | G | A | synonymous_variant | LOW | c.2799G>A|p.Gln933Gln |
S15 S3 |
8 | BAA10g20230 | A10 | 18289547 | G | A | missense_variant | MODERATE | c.2905G>A|p.Gly969Arg |
S94 |
9 | BAA10g20230 | A10 | 18290151 | C | T | missense_variant | MODERATE | c.3509C>T|p.Ala1170Val |
S282 |
10 | BAA10g20230 | A10 | 18291044 | G | A | downstream_gene_variant | MODIFIER | c.*568G>A| |
S292 |