Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18710 | A05 | 10818274 | C | T | upstream_gene_variant | MODIFIER | c.-4750C>T| |
S108 |
2 | BAA05g18710 | A05 | 10818730 | G | A | upstream_gene_variant | MODIFIER | c.-4294G>A| |
S107 |
3 | BAA05g18710 | A05 | 10819021 | G | A | upstream_gene_variant | MODIFIER | c.-4003G>A| |
S205 |
4 | BAA05g18710 | A05 | 10822342 | G | A | upstream_gene_variant | MODIFIER | c.-682G>A| |
S297 |
5 | BAA05g18710 | A05 | 10823170 | G | A | intron_variant | MODIFIER | c.74-28G>A| |
S205 |
6 | BAA05g18710 | A05 | 10823335 | G | A | missense_variant | MODERATE | c.211G>A|p.Asp71Asn |
S156 |
7 | BAA05g18710 | A05 | 10823802 | C | T | intron_variant | MODIFIER | c.599+79C>T| |
S18 |
8 | BAA05g18710 | A05 | 10824346 | C | T | synonymous_variant | LOW | c.834C>T|p.Thr278Thr |
S18 |
9 | BAA05g18710 | A05 | 10824869 | C | T | intron_variant | MODIFIER | c.1224-32C>T| |
S9 |
10 | BAA05g18710 | A05 | 10825797 | G | A | missense_variant | MODERATE | c.1747G>A|p.Gly583Arg |
S243 S299 |
11 | BAA05g18710 | A05 | 10827718 | G | A | downstream_gene_variant | MODIFIER | c.*658G>A| |
S244 |
12 | BAA05g18710 | A05 | 10828461 | C | T | downstream_gene_variant | MODIFIER | c.*1401C>T| |
S183 S198 |
13 | BAA05g18710 | A05 | 10828491 | C | T | downstream_gene_variant | MODIFIER | c.*1431C>T| |
S216 |
14 | BAA05g18710 | A05 | 10828940 | G | A | downstream_gene_variant | MODIFIER | c.*1880G>A| |
S274 |
15 | BAA05g18710 | A05 | 10831869 | C | T | downstream_gene_variant | MODIFIER | c.*4809C>T| |
S270 |