Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02900 | A10 | 1414981 | C | T | upstream_gene_variant | MODIFIER | c.-2223C>T| |
S152 |
2 | BAA10g02900 | A10 | 1415747 | C | T | upstream_gene_variant | MODIFIER | c.-1457C>T| |
S143 |
3 | BAA10g02900 | A10 | 1416171 | G | A | upstream_gene_variant | MODIFIER | c.-1033G>A| |
S302 |
4 | BAA10g02900 | A10 | 1416393 | G | A | upstream_gene_variant | MODIFIER | c.-811G>A| |
S85 |
5 | BAA10g02900 | A10 | 1416661 | G | A | upstream_gene_variant | MODIFIER | c.-543G>A| |
S107 |
6 | BAA10g02900 | A10 | 1417914 | C | T | missense_variant | MODERATE | c.394C>T|p.Leu132Phe |
S60 |
7 | BAA10g02900 | A10 | 1419004 | G | A | downstream_gene_variant | MODIFIER | c.*411G>A| |
S32 |
8 | BAA10g02900 | A10 | 1419887 | G | A | downstream_gene_variant | MODIFIER | c.*1294G>A| |
S48 |
9 | BAA10g02900 | A10 | 1420338 | G | A | downstream_gene_variant | MODIFIER | c.*1745G>A| |
S158 |
10 | BAA10g02900 | A10 | 1420876 | G | A | downstream_gene_variant | MODIFIER | c.*2283G>A| |
S255 |