Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g02780 | A09 | 1769432 | G | A | downstream_gene_variant | MODIFIER | c.*74C>T| |
S302 |
2 | BAA09g02780 | A09 | 1769871 | G | A | missense_variant | MODERATE | c.2683C>T|p.Arg895Cys |
S259 |
3 | BAA09g02780 | A09 | 1770009 | G | A | synonymous_variant | LOW | c.2545C>T|p.Leu849Leu |
S200 |
4 | BAA09g02780 | A09 | 1770227 | G | A | missense_variant | MODERATE | c.2327C>T|p.Pro776Leu |
S40 S49 |
5 | BAA09g02780 | A09 | 1770285 | C | T | missense_variant | MODERATE | c.2269G>A|p.Glu757Lys |
S219 |
6 | BAA09g02780 | A09 | 1770447 | C | T | missense_variant | MODERATE | c.2107G>A|p.Glu703Lys |
S96 |
7 | BAA09g02780 | A09 | 1770458 | G | A | missense_variant | MODERATE | c.2096C>T|p.Ala699Val |
S235 |
8 | BAA09g02780 | A09 | 1770567 | G | A | missense_variant | MODERATE | c.1987C>T|p.Leu663Phe |
S187 |
9 | BAA09g02780 | A09 | 1771998 | C | T | missense_variant | MODERATE | c.556G>A|p.Asp186Asn |
S53 |
10 | BAA09g02780 | A09 | 1772268 | G | A | missense_variant | MODERATE | c.286C>T|p.Leu96Phe |
S146 |
11 | BAA09g02780 | A09 | 1772444 | G | A | missense_variant | MODERATE | c.110C>T|p.Pro37Leu |
S13 |
12 | BAA09g02780 | A09 | 1775813 | T | A | upstream_gene_variant | MODIFIER | c.-3260A>T| |
S109 S282 S289 S5 S75 S8 |