Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04140 | A10 | 2041959 | C | T | downstream_gene_variant | MODIFIER | c.*4183G>A| |
S229 |
2 | BAA10g04140 | A10 | 2042358 | G | A | downstream_gene_variant | MODIFIER | c.*3784C>T| |
S262 |
3 | BAA10g04140 | A10 | 2043403 | G | A | downstream_gene_variant | MODIFIER | c.*2739C>T| |
S1 |
4 | BAA10g04140 | A10 | 2043862 | G | A | downstream_gene_variant | MODIFIER | c.*2280C>T| |
S71 |
5 | BAA10g04140 | A10 | 2043868 | G | A | downstream_gene_variant | MODIFIER | c.*2274C>T| |
S172 |
6 | BAA10g04140 | A10 | 2044819 | C | T | downstream_gene_variant | MODIFIER | c.*1323G>A| |
S206 S26 |
7 | BAA10g04140 | A10 | 2045507 | G | A | downstream_gene_variant | MODIFIER | c.*635C>T| |
S292 |
8 | BAA10g04140 | A10 | 2046280 | C | T | synonymous_variant | LOW | c.879G>A|p.Leu293Leu |
S116 |
9 | BAA10g04140 | A10 | 2046462 | G | A | synonymous_variant | LOW | c.697C>T|p.Leu233Leu |
S46 |