Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11570 | A10 | 13166815 | C | T | missense_variant | MODERATE | c.1789G>A|p.Ala597Thr |
S46 |
2 | BAA10g11570 | A10 | 13166901 | C | T | missense_variant | MODERATE | c.1703G>A|p.Gly568Glu |
S281 |
3 | BAA10g11570 | A10 | 13167605 | G | A | missense_variant | MODERATE | c.1079C>T|p.Pro360Leu |
S111 |
4 | BAA10g11570 | A10 | 13168411 | G | A | missense_variant | MODERATE | c.455C>T|p.Ala152Val |
S82 S92 |
5 | BAA10g11570 | A10 | 13170954 | G | A | upstream_gene_variant | MODIFIER | c.-2089C>T| |
S43 |
6 | BAA10g11570 | A10 | 13171231 | C | T | upstream_gene_variant | MODIFIER | c.-2366G>A| |
S297 |
7 | BAA10g11570 | A10 | 13172223 | C | T | upstream_gene_variant | MODIFIER | c.-3358G>A| |
S270 |