Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g59420 | A09 | 57559515 | G | A | downstream_gene_variant | MODIFIER | c.*1057C>T| |
S291 |
2 | BAA09g59420 | A09 | 57560648 | G | A | missense_variant | MODERATE | c.2189C>T|p.Thr730Met |
S48 |
3 | BAA09g59420 | A09 | 57561364 | C | T | missense_variant | MODERATE | c.1721G>A|p.Ser574Asn |
S150 |
4 | BAA09g59420 | A09 | 57561485 | G | A | synonymous_variant | LOW | c.1600C>T|p.Leu534Leu |
S42 |
5 | BAA09g59420 | A09 | 57561799 | C | T | missense_variant | MODERATE | c.1445G>A|p.Arg482Lys |
S208 S219 |
6 | BAA09g59420 | A09 | 57561924 | C | T | synonymous_variant | LOW | c.1392G>A|p.Gly464Gly |
S99 |
7 | BAA09g59420 | A09 | 57562567 | C | T | missense_variant | MODERATE | c.907G>A|p.Asp303Asn |
S286 |
8 | BAA09g59420 | A09 | 57563761 | C | T | missense_variant | MODERATE | c.322G>A|p.Gly108Arg |
S60 |
9 | BAA09g59420 | A09 | 57564002 | G | A | synonymous_variant | LOW | c.81C>T|p.Val27Val |
S167 |
10 | BAA09g59420 | A09 | 57565054 | G | A | upstream_gene_variant | MODIFIER | c.-972C>T| |
S259 |
11 | BAA09g59420 | A09 | 57565066 | C | T | upstream_gene_variant | MODIFIER | c.-984G>A| |
S180 |
12 | BAA09g59420 | A09 | 57565208 | C | T | upstream_gene_variant | MODIFIER | c.-1126G>A| |
S173 |
13 | BAA09g59420 | A09 | 57565885 | G | A | upstream_gene_variant | MODIFIER | c.-1803C>T| |
S88 |
14 | BAA09g59420 | A09 | 57567685 | G | A | upstream_gene_variant | MODIFIER | c.-3603C>T| |
S297 |