Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g36570 | A02 | 31285712 | C | T | downstream_gene_variant | MODIFIER | c.*4274G>A| |
S201 |
2 | BAA02g36570 | A02 | 31289987 | C | T | splice_region_variant&stop_retained_variant | LOW | c.545G>A|p.Ter182Ter |
S130 |
3 | BAA02g36570 | A02 | 31290090 | G | A | missense_variant | MODERATE | c.442C>T|p.Pro148Ser |
S224 |
4 | BAA02g36570 | A02 | 31290350 | G | A | missense_variant | MODERATE | c.182C>T|p.Thr61Met |
S279 |
5 | BAA02g36570 | A02 | 31290731 | G | A | missense_variant | MODERATE | c.74C>T|p.Thr25Ile |
S72 S78 |
6 | BAA02g36570 | A02 | 31290759 | C | T | missense_variant | MODERATE | c.46G>A|p.Gly16Arg |
S98 |
7 | BAA02g36570 | A02 | 31291657 | C | T | upstream_gene_variant | MODIFIER | c.-853G>A| |
S165 |
8 | BAA02g36570 | A02 | 31293647 | C | T | upstream_gene_variant | MODIFIER | c.-2843G>A| |
S9 |
9 | BAA02g36570 | A02 | 31295695 | G | A | upstream_gene_variant | MODIFIER | c.-4891C>T| |
S228 |