Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66450 | A09 | 60732684 | C | T | synonymous_variant | LOW | c.2625G>A|p.Ala875Ala |
S294 |
2 | BAA09g66450 | A09 | 60733193 | C | T | missense_variant | MODERATE | c.2296G>A|p.Asp766Asn |
S206 S26 |
3 | BAA09g66450 | A09 | 60733653 | G | A | synonymous_variant | LOW | c.1944C>T|p.Val648Val |
S187 |
4 | BAA09g66450 | A09 | 60733986 | C | T | missense_variant | MODERATE | c.1684G>A|p.Asp562Asn |
S28 |
5 | BAA09g66450 | A09 | 60734239 | G | A | synonymous_variant | LOW | c.1533C>T|p.Asp511Asp |
S195 |
6 | BAA09g66450 | A09 | 60735009 | G | A | missense_variant | MODERATE | c.950C>T|p.Ser317Leu |
S115 |
7 | BAA09g66450 | A09 | 60735024 | C | T | missense_variant | MODERATE | c.935G>A|p.Arg312Lys |
S67 |
8 | BAA09g66450 | A09 | 60735479 | G | A | synonymous_variant | LOW | c.480C>T|p.Ser160Ser |
S123 |
9 | BAA09g66450 | A09 | 60735873 | C | T | missense_variant | MODERATE | c.86G>A|p.Arg29Lys |
S41 |
10 | BAA09g66450 | A09 | 60736317 | G | A | upstream_gene_variant | MODIFIER | c.-359C>T| |
S239 |
11 | BAA09g66450 | A09 | 60737115 | C | T | upstream_gene_variant | MODIFIER | c.-1157G>A| |
S217 |
12 | BAA09g66450 | A09 | 60738734 | C | T | upstream_gene_variant | MODIFIER | c.-2776G>A| |
S200 |
13 | BAA09g66450 | A09 | 60738785 | G | A | upstream_gene_variant | MODIFIER | c.-2827C>T| |
S107 |