Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g03780 | A08 | 2647366 | C | T | missense_variant | MODERATE | c.1315G>A|p.Gly439Ser |
S174 S216 S241 |
2 | BAA08g03780 | A08 | 2647758 | G | A | missense_variant | MODERATE | c.923C>T|p.Thr308Met |
S136 |
3 | BAA08g03780 | A08 | 2647868 | C | T | stop_gained | HIGH | c.813G>A|p.Trp271* |
S277 |
4 | BAA08g03780 | A08 | 2647956 | C | T | missense_variant | MODERATE | c.725G>A|p.Arg242Gln |
S99 |
5 | BAA08g03780 | A08 | 2648070 | G | A | missense_variant | MODERATE | c.611C>T|p.Pro204Leu |
S249 |
6 | BAA08g03780 | A08 | 2648311 | C | T | missense_variant | MODERATE | c.370G>A|p.Gly124Ser |
S67 |
7 | BAA08g03780 | A08 | 2649465 | G | A | upstream_gene_variant | MODIFIER | c.-785C>T| |
S240 |
8 | BAA08g03780 | A08 | 2650701 | C | T | upstream_gene_variant | MODIFIER | c.-2021G>A| |
S168 |
9 | BAA08g03780 | A08 | 2651449 | C | T | upstream_gene_variant | MODIFIER | c.-2769G>A| |
S46 |