Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18060 | A05 | 10282667 | C | T | upstream_gene_variant | MODIFIER | c.-4784C>T| |
S113 |
2 | BAA05g18060 | A05 | 10283629 | C | T | upstream_gene_variant | MODIFIER | c.-3822C>T| |
S130 |
3 | BAA05g18060 | A05 | 10284334 | G | A | upstream_gene_variant | MODIFIER | c.-3117G>A| |
S41 |
4 | BAA05g18060 | A05 | 10284338 | G | A | upstream_gene_variant | MODIFIER | c.-3113G>A| |
S241 |
5 | BAA05g18060 | A05 | 10285090 | C | T | upstream_gene_variant | MODIFIER | c.-2361C>T| |
S20 |
6 | BAA05g18060 | A05 | 10285187 | G | A | upstream_gene_variant | MODIFIER | c.-2264G>A| |
S203 |
7 | BAA05g18060 | A05 | 10287133 | G | A | upstream_gene_variant | MODIFIER | c.-318G>A| |
S197 |
8 | BAA05g18060 | A05 | 10287759 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.217-1G>A| |
S34 |
9 | BAA05g18060 | A05 | 10288210 | C | T | synonymous_variant | LOW | c.507C>T|p.Thr169Thr |
S5 |
10 | BAA05g18060 | A05 | 10289563 | C | T | downstream_gene_variant | MODIFIER | c.*291C>T| |
S18 |
11 | BAA05g18060 | A05 | 10289611 | A | T | downstream_gene_variant | MODIFIER | c.*339A>T| |
S156 |
12 | BAA05g18060 | A05 | 10290142 | C | T | downstream_gene_variant | MODIFIER | c.*870C>T| |
S17 |
13 | BAA05g18060 | A05 | 10290416 | G | A | downstream_gene_variant | MODIFIER | c.*1144G>A| |
S298 |
14 | BAA05g18060 | A05 | 10290529 | C | T | downstream_gene_variant | MODIFIER | c.*1257C>T| |
S243 S299 |
15 | BAA05g18060 | A05 | 10290856 | G | A | downstream_gene_variant | MODIFIER | c.*1584G>A| |
S180 |
16 | BAA05g18060 | A05 | 10290896 | G | A | downstream_gene_variant | MODIFIER | c.*1624G>A| |
S293 |
17 | BAA05g18060 | A05 | 10290976 | C | T | downstream_gene_variant | MODIFIER | c.*1704C>T| |
S166 |
18 | BAA05g18060 | A05 | 10291027 | G | A | downstream_gene_variant | MODIFIER | c.*1755G>A| |
S172 S217 |
19 | BAA05g18060 | A05 | 10291169 | G | A | downstream_gene_variant | MODIFIER | c.*1897G>A| |
S23 |