Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00430 | A09 | 473120 | G | A | missense_variant | MODERATE | c.80G>A|p.Arg27Gln |
S130 |
2 | BAA09g00430 | A09 | 473135 | G | A | missense_variant | MODERATE | c.95G>A|p.Gly32Glu |
S163 |
3 | BAA09g00430 | A09 | 473565 | C | T | synonymous_variant | LOW | c.375C>T|p.Leu125Leu |
S272 |
4 | BAA09g00430 | A09 | 473959 | C | T | missense_variant | MODERATE | c.695C>T|p.Thr232Ile |
S77 S82 |
5 | BAA09g00430 | A09 | 473975 | G | A | splice_region_variant&intron_variant | LOW | c.705+6G>A| |
S264 |
6 | BAA09g00430 | A09 | 475772 | C | T | downstream_gene_variant | MODIFIER | c.*562C>T| |
S270 |
7 | BAA09g00430 | A09 | 475833 | C | T | downstream_gene_variant | MODIFIER | c.*623C>T| |
S132 S137 |
8 | BAA09g00430 | A09 | 476116 | G | A | downstream_gene_variant | MODIFIER | c.*906G>A| |
S262 |
9 | BAA09g00430 | A09 | 476404 | G | A | downstream_gene_variant | MODIFIER | c.*1194G>A| |
S163 |