Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42650 | A05 | 40322662 | G | A | downstream_gene_variant | MODIFIER | c.*3635C>T| |
S69 |
2 | BAA05g42650 | A05 | 40323282 | G | A | downstream_gene_variant | MODIFIER | c.*3015C>T| |
S202 |
3 | BAA05g42650 | A05 | 40324004 | C | T | downstream_gene_variant | MODIFIER | c.*2293G>A| |
S251 |
4 | BAA05g42650 | A05 | 40326320 | C | T | missense_variant | MODERATE | c.451G>A|p.Glu151Lys |
S256 |
5 | BAA05g42650 | A05 | 40326362 | C | T | missense_variant | MODERATE | c.409G>A|p.Glu137Lys |
S136 |
6 | BAA05g42650 | A05 | 40326529 | C | T | synonymous_variant | LOW | c.324G>A|p.Gln108Gln |
S107 |
7 | BAA05g42650 | A05 | 40327054 | G | A | synonymous_variant | LOW | c.66C>T|p.Leu22Leu |
S45 |
8 | BAA05g42650 | A05 | 40327095 | C | T | missense_variant | MODERATE | c.25G>A|p.Ala9Thr |
S256 |
9 | BAA05g42650 | A05 | 40327198 | G | A | upstream_gene_variant | MODIFIER | c.-79C>T| |
S16 |
10 | BAA05g42650 | A05 | 40327924 | G | A | upstream_gene_variant | MODIFIER | c.-805C>T| |
S216 |
11 | BAA05g42650 | A05 | 40332053 | G | A | upstream_gene_variant | MODIFIER | c.-4934C>T| |
S79 S91 |