Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g13500 | A09 | 7742782 | C | T | upstream_gene_variant | MODIFIER | c.-855C>T| |
S302 |
2 | BAA09g13500 | A09 | 7743482 | T | G | upstream_gene_variant | MODIFIER | c.-155T>G| |
S213 |
3 | BAA09g13500 | A09 | 7743762 | G | A | synonymous_variant | LOW | c.126G>A|p.Leu42Leu |
S40 S49 |
4 | BAA09g13500 | A09 | 7745178 | C | T | missense_variant | MODERATE | c.866C>T|p.Ser289Phe |
S135 |
5 | BAA09g13500 | A09 | 7745189 | C | T | missense_variant | MODERATE | c.877C>T|p.Pro293Ser |
S36 |
6 | BAA09g13500 | A09 | 7745498 | G | A | missense_variant | MODERATE | c.1186G>A|p.Glu396Lys |
S86 |
7 | BAA09g13500 | A09 | 7746031 | C | T | synonymous_variant | LOW | c.1719C>T|p.Pro573Pro |
S261 |
8 | BAA09g13500 | A09 | 7746487 | G | A | synonymous_variant | LOW | c.2175G>A|p.Gly725Gly |
S229 |
9 | BAA09g13500 | A09 | 7746596 | G | A | missense_variant | MODERATE | c.2284G>A|p.Val762Ile |
S167 |
10 | BAA09g13500 | A09 | 7746950 | C | T | missense_variant | MODERATE | c.2638C>T|p.Leu880Phe |
S153 |
11 | BAA09g13500 | A09 | 7747461 | G | A | synonymous_variant | LOW | c.2874G>A|p.Ala958Ala |
S20 |