Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17130 | A10 | 16643804 | G | A | downstream_gene_variant | MODIFIER | c.*741C>T| |
S132 S137 S215 |
2 | BAA10g17130 | A10 | 16644382 | C | T | downstream_gene_variant | MODIFIER | c.*163G>A| |
S116 |
3 | BAA10g17130 | A10 | 16644678 | G | A | missense_variant | MODERATE | c.344C>T|p.Pro115Leu |
S10 |
4 | BAA10g17130 | A10 | 16645205 | G | A | upstream_gene_variant | MODIFIER | c.-184C>T| |
S128 |
5 | BAA10g17130 | A10 | 16646209 | C | T | upstream_gene_variant | MODIFIER | c.-1188G>A| |
S282 |
6 | BAA10g17130 | A10 | 16647367 | C | T | upstream_gene_variant | MODIFIER | c.-2346G>A| |
S115 |
7 | BAA10g17130 | A10 | 16647870 | C | T | upstream_gene_variant | MODIFIER | c.-2849G>A| |
S197 |
8 | BAA10g17130 | A10 | 16648352 | G | A | upstream_gene_variant | MODIFIER | c.-3331C>T| |
S71 |
9 | BAA10g17130 | A10 | 16649984 | C | T | upstream_gene_variant | MODIFIER | c.-4963G>A| |
S174 S27 S39 |