Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g02590 | A03 | 1145681 | G | A | upstream_gene_variant | MODIFIER | c.-4859G>A| |
S67 |
2 | BAA03g02590 | A03 | 1146516 | C | T | upstream_gene_variant | MODIFIER | c.-4024C>T| |
S199 |
3 | BAA03g02590 | A03 | 1146672 | C | T | upstream_gene_variant | MODIFIER | c.-3868C>T| |
S159 S243 |
4 | BAA03g02590 | A03 | 1146860 | C | T | upstream_gene_variant | MODIFIER | c.-3680C>T| |
S128 |
5 | BAA03g02590 | A03 | 1148263 | C | T | upstream_gene_variant | MODIFIER | c.-2277C>T| |
S218 |
6 | BAA03g02590 | A03 | 1148338 | C | T | upstream_gene_variant | MODIFIER | c.-2202C>T| |
S223 |
7 | BAA03g02590 | A03 | 1148632 | C | T | upstream_gene_variant | MODIFIER | c.-1908C>T| |
S263 |
8 | BAA03g02590 | A03 | 1150408 | C | T | upstream_gene_variant | MODIFIER | c.-132C>T| |
S221 |
9 | BAA03g02590 | A03 | 1150651 | G | A | missense_variant | MODERATE | c.112G>A|p.Val38Ile |
S16 |
10 | BAA03g02590 | A03 | 1150788 | C | T | synonymous_variant | LOW | c.249C>T|p.Asp83Asp |
S129 |
11 | BAA03g02590 | A03 | 1150848 | G | A | synonymous_variant | LOW | c.309G>A|p.Leu103Leu |
S301 S304 |
12 | BAA03g02590 | A03 | 1150871 | T | C | missense_variant | MODERATE | c.332T>C|p.Met111Thr |
S57 |
13 | BAA03g02590 | A03 | 1153125 | G | A | downstream_gene_variant | MODIFIER | c.*2172G>A| |
S275 |
14 | BAA03g02590 | A03 | 1154456 | C | T | downstream_gene_variant | MODIFIER | c.*3503C>T| |
S270 |