Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11460 | A01 | 5306041 | G | A | synonymous_variant | LOW | c.417G>A|p.Arg139Arg |
S59 |
2 | BAA01g11460 | A01 | 5306162 | G | A | missense_variant | MODERATE | c.538G>A|p.Gly180Arg |
S139 |
3 | BAA01g11460 | A01 | 5307917 | G | A | missense_variant | MODERATE | c.1586G>A|p.Cys529Tyr |
S263 |
4 | BAA01g11460 | A01 | 5309325 | C | T | missense_variant | MODERATE | c.2323C>T|p.Pro775Ser |
S76 |
5 | BAA01g11460 | A01 | 5310005 | C | T | synonymous_variant | LOW | c.2748C>T|p.Thr916Thr |
S203 |
6 | BAA01g11460 | A01 | 5311120 | C | T | synonymous_variant | LOW | c.3291C>T|p.Val1097Val |
S247 |
7 | BAA01g11460 | A01 | 5313842 | C | T | downstream_gene_variant | MODIFIER | c.*2587C>T| |
S71 |
8 | BAA01g11460 | A01 | 5314491 | C | T | downstream_gene_variant | MODIFIER | c.*3236C>T| |
S202 |
9 | BAA01g11460 | A01 | 5314683 | G | A | downstream_gene_variant | MODIFIER | c.*3428G>A| |
S81 S85 |
10 | BAA01g11460 | A01 | 5315057 | C | T | downstream_gene_variant | MODIFIER | c.*3802C>T| |
S260 S42 |