Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16990 | A09 | 10088572 | C | T | missense_variant | MODERATE | c.883G>A|p.Glu295Lys |
S289 S290 |
2 | BAA09g16990 | A09 | 10088893 | G | A | missense_variant | MODERATE | c.562C>T|p.His188Tyr |
S291 |
3 | BAA09g16990 | A09 | 10089378 | G | A | missense_variant | MODERATE | c.77C>T|p.Pro26Leu |
S70 |
4 | BAA09g16990 | A09 | 10089869 | C | T | upstream_gene_variant | MODIFIER | c.-415G>A| |
S140 |
5 | BAA09g16990 | A09 | 10089920 | C | T | upstream_gene_variant | MODIFIER | c.-466G>A| |
S36 |
6 | BAA09g16990 | A09 | 10090487 | T | G | upstream_gene_variant | MODIFIER | c.-1033A>C| |
S306 |
7 | BAA09g16990 | A09 | 10090489 | C | T | upstream_gene_variant | MODIFIER | c.-1035G>A| |
S28 |
8 | BAA09g16990 | A09 | 10090620 | G | A | upstream_gene_variant | MODIFIER | c.-1166C>T| |
S255 |
9 | BAA09g16990 | A09 | 10091623 | G | A | upstream_gene_variant | MODIFIER | c.-2169C>T| |
S25 |
10 | BAA09g16990 | A09 | 10092287 | C | T | upstream_gene_variant | MODIFIER | c.-2833G>A| |
S231 |
11 | BAA09g16990 | A09 | 10092405 | G | A | upstream_gene_variant | MODIFIER | c.-2951C>T| |
S130 |