Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18060 | A01 | 8837398 | T | A | downstream_gene_variant | MODIFIER | c.*1548A>T| |
S241 |
2 | BAA01g18060 | A01 | 8840097 | T | C | missense_variant | MODERATE | c.1118A>G|p.Glu373Gly |
S255 |
3 | BAA01g18060 | A01 | 8840118 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1098-1G>A| |
S247 |
4 | BAA01g18060 | A01 | 8840237 | C | T | missense_variant | MODERATE | c.1064G>A|p.Arg355Lys |
S167 |
5 | BAA01g18060 | A01 | 8840920 | G | A | intron_variant | MODIFIER | c.688-151C>T| |
S172 S217 |
6 | BAA01g18060 | A01 | 8842003 | C | T | missense_variant | MODERATE | c.589G>A|p.Gly197Arg |
S182 |
7 | BAA01g18060 | A01 | 8842349 | G | A | splice_region_variant&intron_variant | LOW | c.450+3C>T| |
S45 |
8 | BAA01g18060 | A01 | 8842856 | G | A | intron_variant | MODIFIER | c.175-15C>T| |
S156 |
9 | BAA01g18060 | A01 | 8842942 | G | A | intron_variant | MODIFIER | c.175-101C>T| |
S246 |
10 | BAA01g18060 | A01 | 8843846 | G | A | upstream_gene_variant | MODIFIER | c.-616C>T| |
S209 |
11 | BAA01g18060 | A01 | 8845073 | C | T | upstream_gene_variant | MODIFIER | c.-1843G>A| |
S223 |
12 | BAA01g18060 | A01 | 8845235 | C | T | upstream_gene_variant | MODIFIER | c.-2005G>A| |
S146 |
13 | BAA01g18060 | A01 | 8847091 | C | T | upstream_gene_variant | MODIFIER | c.-3861G>A| |
S286 |
14 | BAA01g18060 | A01 | 8847597 | C | T | upstream_gene_variant | MODIFIER | c.-4367G>A| |
S71 |
15 | BAA01g18060 | A01 | 8847918 | C | T | upstream_gene_variant | MODIFIER | c.-4688G>A| |
S47 |