Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26080 | A02 | 14446736 | C | T | upstream_gene_variant | MODIFIER | c.-365C>T| |
S61 |
2 | BAA02g26080 | A02 | 14447377 | C | T | missense_variant | MODERATE | c.277C>T|p.Leu93Phe |
S192 |
3 | BAA02g26080 | A02 | 14447727 | G | A | missense_variant | MODERATE | c.538G>A|p.Asp180Asn |
S28 S50 |
4 | BAA02g26080 | A02 | 14447729 | C | T | synonymous_variant | LOW | c.540C>T|p.Asp180Asp |
S32 |
5 | BAA02g26080 | A02 | 14447786 | G | A | missense_variant | MODERATE | c.597G>A|p.Met199Ile |
S95 |
6 | BAA02g26080 | A02 | 14449527 | G | T | downstream_gene_variant | MODIFIER | c.*999G>T| |
S99 |
7 | BAA02g26080 | A02 | 14450160 | G | A | downstream_gene_variant | MODIFIER | c.*1632G>A| |
S298 |
8 | BAA02g26080 | A02 | 14450991 | C | T | downstream_gene_variant | MODIFIER | c.*2463C>T| |
S183 S198 |
9 | BAA02g26080 | A02 | 14451734 | C | T | downstream_gene_variant | MODIFIER | c.*3206C>T| |
S216 |
10 | BAA02g26080 | A02 | 14452728 | C | T | downstream_gene_variant | MODIFIER | c.*4200C>T| |
S139 |
11 | BAA02g26080 | A02 | 14453237 | G | A | downstream_gene_variant | MODIFIER | c.*4709G>A| |
S217 |