Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01540 | A09 | 1093282 | G | A | missense_variant | MODERATE | c.91G>A|p.Glu31Lys |
S299 |
2 | BAA09g01540 | A09 | 1093713 | C | T | splice_region_variant&synonymous_variant | LOW | c.162C>T|p.Asp54Asp |
S18 |
3 | BAA09g01540 | A09 | 1093822 | G | A | missense_variant | MODERATE | c.271G>A|p.Glu91Lys |
S108 |
4 | BAA09g01540 | A09 | 1095717 | C | T | stop_gained | HIGH | c.1255C>T|p.Gln419* |
S171 |
5 | BAA09g01540 | A09 | 1095744 | G | A | missense_variant | MODERATE | c.1282G>A|p.Gly428Arg |
S187 |
6 | BAA09g01540 | A09 | 1096620 | G | A | synonymous_variant | LOW | c.1917G>A|p.Lys639Lys |
S162 |
7 | BAA09g01540 | A09 | 1098525 | C | T | downstream_gene_variant | MODIFIER | c.*1589C>T| |
S143 |
8 | BAA09g01540 | A09 | 1098710 | C | T | downstream_gene_variant | MODIFIER | c.*1774C>T| |
S230 |
9 | BAA09g01540 | A09 | 1099669 | G | A | downstream_gene_variant | MODIFIER | c.*2733G>A| |
S166 |