Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g43970 | A01 | 29100823 | C | T | downstream_gene_variant | MODIFIER | c.*3012G>A| |
S182 |
2 | BAA01g43970 | A01 | 29105445 | C | T | missense_variant&splice_region_variant | MODERATE | c.1546G>A|p.Glu516Lys |
S182 |
3 | BAA01g43970 | A01 | 29105579 | G | A | missense_variant | MODERATE | c.1483C>T|p.His495Tyr |
S232 |
4 | BAA01g43970 | A01 | 29106304 | C | T | splice_region_variant&intron_variant | LOW | c.1460+4G>A| |
S301 S304 |
5 | BAA01g43970 | A01 | 29106411 | G | A | synonymous_variant | LOW | c.1357C>T|p.Leu453Leu |
S122 |
6 | BAA01g43970 | A01 | 29107089 | G | A | stop_gained | HIGH | c.679C>T|p.Arg227* |
S117 |
7 | BAA01g43970 | A01 | 29107109 | C | T | missense_variant | MODERATE | c.659G>A|p.Gly220Glu |
S240 |
8 | BAA01g43970 | A01 | 29107692 | C | T | missense_variant | MODERATE | c.76G>A|p.Glu26Lys |
S68 |
9 | BAA01g43970 | A01 | 29108015 | C | T | upstream_gene_variant | MODIFIER | c.-248G>A| |
S275 |
10 | BAA01g43970 | A01 | 29108078 | G | A | upstream_gene_variant | MODIFIER | c.-311C>T| |
S241 |
11 | BAA01g43970 | A01 | 29108424 | C | T | upstream_gene_variant | MODIFIER | c.-657G>A| |
S44 |
12 | BAA01g43970 | A01 | 29109085 | C | T | upstream_gene_variant | MODIFIER | c.-1318G>A| |
S294 |