Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15520 | A02 | 7488028 | C | T | missense_variant | MODERATE | c.107C>T|p.Thr36Ile |
S135 |
2 | BAA02g15520 | A02 | 7488099 | G | A | missense_variant | MODERATE | c.178G>A|p.Glu60Lys |
S125 |
3 | BAA02g15520 | A02 | 7488218 | C | T | synonymous_variant | LOW | c.297C>T|p.Asp99Asp |
S182 |
4 | BAA02g15520 | A02 | 7488540 | G | A | missense_variant | MODERATE | c.619G>A|p.Val207Ile |
S193 |
5 | BAA02g15520 | A02 | 7488696 | G | A | missense_variant | MODERATE | c.775G>A|p.Glu259Lys |
S202 |
6 | BAA02g15520 | A02 | 7489432 | C | T | synonymous_variant | LOW | c.1281C>T|p.Leu427Leu |
S111 S127 |
7 | BAA02g15520 | A02 | 7491827 | G | A | downstream_gene_variant | MODIFIER | c.*2293G>A| |
S260 |
8 | BAA02g15520 | A02 | 7492953 | G | A | downstream_gene_variant | MODIFIER | c.*3419G>A| |
S67 |
9 | BAA02g15520 | A02 | 7493411 | G | A | downstream_gene_variant | MODIFIER | c.*3877G>A| |
S169 |
10 | BAA02g15520 | A02 | 7493511 | C | T | downstream_gene_variant | MODIFIER | c.*3977C>T| |
S13 |
11 | BAA02g15520 | A02 | 7493612 | C | T | downstream_gene_variant | MODIFIER | c.*4078C>T| |
S158 |