Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35900 | A09 | 44200020 | C | T | upstream_gene_variant | MODIFIER | c.-4463C>T| |
S255 |
2 | BAA09g35900 | A09 | 44200610 | C | T | upstream_gene_variant | MODIFIER | c.-3873C>T| |
S191 |
3 | BAA09g35900 | A09 | 44204496 | C | T | missense_variant | MODERATE | c.14C>T|p.Thr5Met |
S247 |
4 | BAA09g35900 | A09 | 44204505 | C | T | missense_variant | MODERATE | c.23C>T|p.Thr8Ile |
S32 |
5 | BAA09g35900 | A09 | 44204514 | G | A | missense_variant | MODERATE | c.32G>A|p.Arg11Lys |
S70 |
6 | BAA09g35900 | A09 | 44205823 | C | T | synonymous_variant | LOW | c.1341C>T|p.Leu447Leu |
S303 |
7 | BAA09g35900 | A09 | 44206046 | G | A | missense_variant | MODERATE | c.1564G>A|p.Gly522Arg |
S244 |
8 | BAA09g35900 | A09 | 44208568 | C | T | downstream_gene_variant | MODIFIER | c.*2496C>T| |
S158 |
9 | BAA09g35900 | A09 | 44208622 | G | A | downstream_gene_variant | MODIFIER | c.*2550G>A| |
S87 |