Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g33600 | A09 | 42168676 | C | T | missense_variant | MODERATE | c.232G>A|p.Val78Ile |
S96 |
2 | BAA09g33600 | A09 | 42171862 | C | T | upstream_gene_variant | MODIFIER | c.-2955G>A| |
S255 |
3 | BAA09g33600 | A09 | 42171926 | G | A | upstream_gene_variant | MODIFIER | c.-3019C>T| |
S12 |
4 | BAA09g33600 | A09 | 42172193 | C | T | upstream_gene_variant | MODIFIER | c.-3286G>A| |
S50 |
5 | BAA09g33600 | A09 | 42173077 | C | T | upstream_gene_variant | MODIFIER | c.-4170G>A| |
S305 |
6 | BAA09g33600 | A09 | 42173549 | G | A | upstream_gene_variant | MODIFIER | c.-4642C>T| |
S137 S215 |
7 | BAA09g33600 | A09 | 42173564 | T | A | upstream_gene_variant | MODIFIER | c.-4657A>T| |
S188 |
8 | BAA09g33600 | A09 | 42173785 | C | T | upstream_gene_variant | MODIFIER | c.-4878G>A| |
S202 S256 |
9 | BAA09g33600 | A09 | 42173787 | G | A | upstream_gene_variant | MODIFIER | c.-4880C>T| |
S12 |
10 | BAA09g33600 | A09 | 42173851 | G | A | upstream_gene_variant | MODIFIER | c.-4944C>T| |
S177 |