Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00750 | A05 | 426017 | C | T | upstream_gene_variant | MODIFIER | c.-3649C>T| |
S162 |
2 | BAA05g00750 | A05 | 426638 | C | T | upstream_gene_variant | MODIFIER | c.-3028C>T| |
S271 |
3 | BAA05g00750 | A05 | 427195 | G | A | upstream_gene_variant | MODIFIER | c.-2471G>A| |
S224 |
4 | BAA05g00750 | A05 | 427940 | G | A | upstream_gene_variant | MODIFIER | c.-1726G>A| |
S23 |
5 | BAA05g00750 | A05 | 428026 | G | A | upstream_gene_variant | MODIFIER | c.-1640G>A| |
S272 |
6 | BAA05g00750 | A05 | 428633 | G | A | upstream_gene_variant | MODIFIER | c.-1033G>A| |
S6 |
7 | BAA05g00750 | A05 | 428677 | G | A | upstream_gene_variant | MODIFIER | c.-989G>A| |
S76 |
8 | BAA05g00750 | A05 | 429164 | C | T | upstream_gene_variant | MODIFIER | c.-502C>T| |
S51 |
9 | BAA05g00750 | A05 | 430208 | C | T | stop_gained | HIGH | c.214C>T|p.Gln72* |
S160 |
10 | BAA05g00750 | A05 | 430607 | C | T | missense_variant | MODERATE | c.535C>T|p.Pro179Ser |
S20 |
11 | BAA05g00750 | A05 | 430665 | C | T | missense_variant | MODERATE | c.593C>T|p.Ser198Phe |
S54 |