Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g23000 | A08 | 17124304 | C | T | upstream_gene_variant | MODIFIER | c.-1756C>T| |
S280 |
2 | BAA08g23000 | A08 | 17125565 | C | T | upstream_gene_variant | MODIFIER | c.-495C>T| |
S142 |
3 | BAA08g23000 | A08 | 17126261 | G | A | missense_variant | MODERATE | c.202G>A|p.Glu68Lys |
S100 |
4 | BAA08g23000 | A08 | 17126489 | G | A | missense_variant | MODERATE | c.430G>A|p.Glu144Lys |
S286 |
5 | BAA08g23000 | A08 | 17126521 | G | A | splice_region_variant&synonymous_variant | LOW | c.462G>A|p.Gln154Gln |
S92 |
6 | BAA08g23000 | A08 | 17127352 | G | A | missense_variant | MODERATE | c.671G>A|p.Gly224Glu |
S46 |
7 | BAA08g23000 | A08 | 17127735 | G | A | missense_variant | MODERATE | c.1054G>A|p.Gly352Ser |
S78 |
8 | BAA08g23000 | A08 | 17131567 | G | A | downstream_gene_variant | MODIFIER | c.*3776G>A| |
S151 S263 |
9 | BAA08g23000 | A08 | 17132779 | C | T | downstream_gene_variant | MODIFIER | c.*4988C>T| |
S135 |