Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19430 | A10 | 17812917 | C | T | stop_gained | HIGH | c.1497G>A|p.Trp499* |
S46 |
2 | BAA10g19430 | A10 | 17813022 | G | A | missense_variant | MODERATE | c.1462C>T|p.Leu488Phe |
S174 |
3 | BAA10g19430 | A10 | 17814502 | G | A | intron_variant | MODIFIER | c.514-50C>T| |
S72 S78 |
4 | BAA10g19430 | A10 | 17814767 | G | A | intron_variant | MODIFIER | c.384+37C>T| |
S28 |
5 | BAA10g19430 | A10 | 17814839 | C | T | missense_variant | MODERATE | c.349G>A|p.Gly117Arg |
S18 |
6 | BAA10g19430 | A10 | 17814972 | C | T | missense_variant | MODERATE | c.280G>A|p.Ala94Thr |
S18 |
7 | BAA10g19430 | A10 | 17815786 | G | A | upstream_gene_variant | MODIFIER | c.-231C>T| |
S289 S290 |
8 | BAA10g19430 | A10 | 17816840 | G | A | upstream_gene_variant | MODIFIER | c.-1285C>T| |
S261 |
9 | BAA10g19430 | A10 | 17819101 | C | T | upstream_gene_variant | MODIFIER | c.-3546G>A| |
S199 |
10 | BAA10g19430 | A10 | 17820405 | G | A | upstream_gene_variant | MODIFIER | c.-4850C>T| |
S162 |