Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01080 | A09 | 787558 | G | A | missense_variant | MODERATE | c.1360C>T|p.Pro454Ser |
S162 |
2 | BAA09g01080 | A09 | 787569 | G | A | missense_variant | MODERATE | c.1349C>T|p.Pro450Leu |
S136 |
3 | BAA09g01080 | A09 | 789218 | C | T | missense_variant | MODERATE | c.202G>A|p.Gly68Arg |
S20 |
4 | BAA09g01080 | A09 | 789373 | C | T | missense_variant | MODERATE | c.47G>A|p.Gly16Asp |
S158 |
5 | BAA09g01080 | A09 | 789651 | G | A | upstream_gene_variant | MODIFIER | c.-232C>T| |
S296 |
6 | BAA09g01080 | A09 | 790406 | G | A | upstream_gene_variant | MODIFIER | c.-987C>T| |
S124 |
7 | BAA09g01080 | A09 | 790810 | C | T | upstream_gene_variant | MODIFIER | c.-1391G>A| |
S40 S49 |
8 | BAA09g01080 | A09 | 791047 | G | A | upstream_gene_variant | MODIFIER | c.-1628C>T| |
S156 S34 S6 |
9 | BAA09g01080 | A09 | 792371 | C | T | upstream_gene_variant | MODIFIER | c.-2952G>A| |
S134 |
10 | BAA09g01080 | A09 | 792619 | C | T | upstream_gene_variant | MODIFIER | c.-3200G>A| |
S86 |
11 | BAA09g01080 | A09 | 794015 | C | T | upstream_gene_variant | MODIFIER | c.-4596G>A| |
S182 |