Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g33390 | A05 | 35110974 | C | T | missense_variant | MODERATE | c.1457G>A|p.Arg486Lys |
S182 |
2 | BAA05g33390 | A05 | 35111263 | G | A | missense_variant | MODERATE | c.1331C>T|p.Pro444Leu |
S201 |
3 | BAA05g33390 | A05 | 35111870 | C | T | missense_variant&splice_region_variant | MODERATE | c.1037G>A|p.Gly346Asp |
S294 |
4 | BAA05g33390 | A05 | 35113020 | C | T | missense_variant&splice_region_variant | MODERATE | c.373G>A|p.Gly125Ser |
S202 |
5 | BAA05g33390 | A05 | 35113601 | C | T | missense_variant | MODERATE | c.185G>A|p.Cys62Tyr |
S35 |
6 | BAA05g33390 | A05 | 35115313 | C | T | upstream_gene_variant | MODIFIER | c.-1014G>A| |
S143 |
7 | BAA05g33390 | A05 | 35115331 | G | A | upstream_gene_variant | MODIFIER | c.-1032C>T| |
S158 |
8 | BAA05g33390 | A05 | 35115621 | C | T | upstream_gene_variant | MODIFIER | c.-1322G>A| |
S174 |
9 | BAA05g33390 | A05 | 35115911 | C | T | upstream_gene_variant | MODIFIER | c.-1612G>A| |
S239 |
10 | BAA05g33390 | A05 | 35118118 | G | A | upstream_gene_variant | MODIFIER | c.-3819C>T| |
S168 |
11 | BAA05g33390 | A05 | 35119124 | G | A | upstream_gene_variant | MODIFIER | c.-4825C>T| |
S119 |