Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16680 | A09 | 9791812 | A | T | downstream_gene_variant | MODIFIER | c.*1615T>A| |
S133 S202 |
2 | BAA09g16680 | A09 | 9793542 | G | A | missense_variant | MODERATE | c.806C>T|p.Thr269Ile |
S240 |
3 | BAA09g16680 | A09 | 9793674 | G | A | missense_variant | MODERATE | c.674C>T|p.Ala225Val |
S65 |
4 | BAA09g16680 | A09 | 9793693 | G | A | missense_variant | MODERATE | c.655C>T|p.Pro219Ser |
S12 |
5 | BAA09g16680 | A09 | 9793885 | G | A | missense_variant | MODERATE | c.463C>T|p.Pro155Ser |
S77 S82 |
6 | BAA09g16680 | A09 | 9793987 | G | A | missense_variant | MODERATE | c.361C>T|p.Pro121Ser |
S113 |
7 | BAA09g16680 | A09 | 9794082 | C | T | missense_variant | MODERATE | c.266G>A|p.Gly89Asp |
S171 |
8 | BAA09g16680 | A09 | 9794248 | G | A | missense_variant | MODERATE | c.100C>T|p.His34Tyr |
S172 S217 |
9 | BAA09g16680 | A09 | 9795325 | C | T | upstream_gene_variant | MODIFIER | c.-978G>A| |
S217 |
10 | BAA09g16680 | A09 | 9795967 | G | A | upstream_gene_variant | MODIFIER | c.-1620C>T| |
S247 |
11 | BAA09g16680 | A09 | 9796146 | C | T | upstream_gene_variant | MODIFIER | c.-1799G>A| |
S287 |
12 | BAA09g16680 | A09 | 9796603 | C | T | upstream_gene_variant | MODIFIER | c.-2256G>A| |
S132 S137 |
13 | BAA09g16680 | A09 | 9797219 | C | T | upstream_gene_variant | MODIFIER | c.-2872G>A| |
S17 |
14 | BAA09g16680 | A09 | 9798787 | G | A | upstream_gene_variant | MODIFIER | c.-4440C>T| |
S79 S84 |