Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g38990 | A05 | 38204957 | G | A | missense_variant | MODERATE | c.1792C>T|p.Pro598Ser |
S308 |
2 | BAA05g38990 | A05 | 38205126 | C | T | missense_variant | MODERATE | c.1698G>A|p.Met566Ile |
S72 S78 |
3 | BAA05g38990 | A05 | 38205485 | A | G | synonymous_variant | LOW | c.1419T>C|p.Ile473Ile |
S110 S82 S92 |
4 | BAA05g38990 | A05 | 38206777 | C | T | synonymous_variant | LOW | c.618G>A|p.Glu206Glu |
S171 |
5 | BAA05g38990 | A05 | 38206829 | G | A | missense_variant | MODERATE | c.566C>T|p.Pro189Leu |
S205 |
6 | BAA05g38990 | A05 | 38207899 | C | T | missense_variant | MODERATE | c.130G>A|p.Glu44Lys |
S242 |
7 | BAA05g38990 | A05 | 38208802 | G | A | upstream_gene_variant | MODIFIER | c.-437C>T| |
S107 |
8 | BAA05g38990 | A05 | 38208871 | G | A | upstream_gene_variant | MODIFIER | c.-506C>T| |
S95 |
9 | BAA05g38990 | A05 | 38209028 | G | A | upstream_gene_variant | MODIFIER | c.-663C>T| |
S117 |
10 | BAA05g38990 | A05 | 38209321 | G | A | upstream_gene_variant | MODIFIER | c.-956C>T| |
S134 |
11 | BAA05g38990 | A05 | 38209395 | C | T | upstream_gene_variant | MODIFIER | c.-1030G>A| |
S37 |
12 | BAA05g38990 | A05 | 38209524 | C | T | upstream_gene_variant | MODIFIER | c.-1159G>A| |
S129 |