Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17630 | A05 | 9937266 | G | A | downstream_gene_variant | MODIFIER | c.*4680C>T| |
S218 S267 |
2 | BAA05g17630 | A05 | 9938600 | C | T | downstream_gene_variant | MODIFIER | c.*3346G>A| |
S166 |
3 | BAA05g17630 | A05 | 9939040 | G | A | downstream_gene_variant | MODIFIER | c.*2906C>T| |
S46 |
4 | BAA05g17630 | A05 | 9941988 | G | A | synonymous_variant | LOW | c.2250C>T|p.Asn750Asn |
S151 S263 |
5 | BAA05g17630 | A05 | 9942510 | G | A | synonymous_variant | LOW | c.1728C>T|p.Leu576Leu |
S231 |
6 | BAA05g17630 | A05 | 9942875 | C | T | missense_variant | MODERATE | c.1363G>A|p.Gly455Arg |
S18 |
7 | BAA05g17630 | A05 | 9943114 | G | A | synonymous_variant | LOW | c.1188C>T|p.Thr396Thr |
S64 |
8 | BAA05g17630 | A05 | 9943256 | G | A | intron_variant | MODIFIER | c.1085+35C>T| |
S161 |
9 | BAA05g17630 | A05 | 9945497 | C | T | missense_variant | MODERATE | c.79G>A|p.Gly27Ser |
S45 |
10 | BAA05g17630 | A05 | 9947420 | G | A | upstream_gene_variant | MODIFIER | c.-1845C>T| |
S46 |
11 | BAA05g17630 | A05 | 9949935 | G | A | upstream_gene_variant | MODIFIER | c.-4360C>T| |
S64 |
12 | BAA05g17630 | A05 | 9950053 | C | T | upstream_gene_variant | MODIFIER | c.-4478G>A| |
S28 |