Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34120 | A02 | 29265052 | C | T | upstream_gene_variant | MODIFIER | c.-4218C>T| |
S40 S49 |
2 | BAA02g34120 | A02 | 29265208 | C | T | upstream_gene_variant | MODIFIER | c.-4062C>T| |
S135 |
3 | BAA02g34120 | A02 | 29270115 | C | T | missense_variant | MODERATE | c.505C>T|p.Pro169Ser |
S171 |
4 | BAA02g34120 | A02 | 29271236 | C | T | synonymous_variant | LOW | c.1216C>T|p.Leu406Leu |
S172 S217 |
5 | BAA02g34120 | A02 | 29271410 | G | A | missense_variant | MODERATE | c.1390G>A|p.Glu464Lys |
S224 |
6 | BAA02g34120 | A02 | 29271463 | C | T | synonymous_variant | LOW | c.1443C>T|p.Val481Val |
S123 |
7 | BAA02g34120 | A02 | 29271684 | C | T | missense_variant | MODERATE | c.1592C>T|p.Pro531Leu |
S46 |
8 | BAA02g34120 | A02 | 29271824 | G | A | splice_region_variant&intron_variant | LOW | c.1660-7G>A| |
S36 |
9 | BAA02g34120 | A02 | 29271828 | C | T | splice_region_variant&intron_variant | LOW | c.1660-3C>T| |
S124 |
10 | BAA02g34120 | A02 | 29273220 | C | T | downstream_gene_variant | MODIFIER | c.*1068C>T| |
S42 |
11 | BAA02g34120 | A02 | 29273392 | C | T | downstream_gene_variant | MODIFIER | c.*1240C>T| |
S266 |
12 | BAA02g34120 | A02 | 29273865 | C | T | downstream_gene_variant | MODIFIER | c.*1713C>T| |
S301 S304 |