Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38220 | A09 | 46195669 | C | T | missense_variant | MODERATE | c.1679G>A|p.Arg560Lys |
S232 |
2 | BAA09g38220 | A09 | 46195744 | C | T | missense_variant | MODERATE | c.1604G>A|p.Arg535Lys |
S193 |
3 | BAA09g38220 | A09 | 46197362 | G | A | synonymous_variant | LOW | c.784C>T|p.Leu262Leu |
S186 |
4 | BAA09g38220 | A09 | 46197753 | C | T | missense_variant | MODERATE | c.593G>A|p.Arg198Lys |
S183 S198 |
5 | BAA09g38220 | A09 | 46198306 | G | A | missense_variant | MODERATE | c.311C>T|p.Ala104Val |
S89 |
6 | BAA09g38220 | A09 | 46198591 | G | A | synonymous_variant | LOW | c.201C>T|p.Tyr67Tyr |
S273 |
7 | BAA09g38220 | A09 | 46199201 | G | A | synonymous_variant | LOW | c.159C>T|p.Val53Val |
S172 S217 |
8 | BAA09g38220 | A09 | 46200141 | C | T | upstream_gene_variant | MODIFIER | c.-782G>A| |
S180 |
9 | BAA09g38220 | A09 | 46200296 | C | T | upstream_gene_variant | MODIFIER | c.-937G>A| |
S104 S52 |
10 | BAA09g38220 | A09 | 46200709 | C | T | upstream_gene_variant | MODIFIER | c.-1350G>A| |
S18 |
11 | BAA09g38220 | A09 | 46202236 | C | T | upstream_gene_variant | MODIFIER | c.-2877G>A| |
S239 |
12 | BAA09g38220 | A09 | 46202601 | C | T | upstream_gene_variant | MODIFIER | c.-3242G>A| |
S180 |
13 | BAA09g38220 | A09 | 46203276 | C | T | upstream_gene_variant | MODIFIER | c.-3917G>A| |
S219 S72 |
14 | BAA09g38220 | A09 | 46203439 | C | T | upstream_gene_variant | MODIFIER | c.-4080G>A| |
S213 |
15 | BAA09g38220 | A09 | 46204182 | C | T | upstream_gene_variant | MODIFIER | c.-4823G>A| |
S223 |