Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19020 | A10 | 17604334 | G | T | missense_variant | MODERATE | c.200C>A|p.Ser67Tyr |
S134 |
2 | BAA10g19020 | A10 | 17604342 | C | T | synonymous_variant | LOW | c.192G>A|p.Glu64Glu |
S243 |
3 | BAA10g19020 | A10 | 17604580 | G | A | missense_variant | MODERATE | c.31C>T|p.His11Tyr |
S223 |
4 | BAA10g19020 | A10 | 17608942 | G | A | upstream_gene_variant | MODIFIER | c.-4332C>T| |
S148 S210 |
5 | BAA10g19020 | A10 | 17609015 | C | T | upstream_gene_variant | MODIFIER | c.-4405G>A| |
S113 |