Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65950 | A09 | 60499592 | C | T | downstream_gene_variant | MODIFIER | c.*3951G>A| |
S245 |
2 | BAA09g65950 | A09 | 60503994 | G | A | missense_variant | MODERATE | c.311C>T|p.Pro104Leu |
S2 |
3 | BAA09g65950 | A09 | 60504287 | G | A | missense_variant | MODERATE | c.239C>T|p.Ala80Val |
S46 |
4 | BAA09g65950 | A09 | 60505756 | C | T | upstream_gene_variant | MODIFIER | c.-1019G>A| |
S245 |
5 | BAA09g65950 | A09 | 60506136 | G | A | upstream_gene_variant | MODIFIER | c.-1399C>T| |
S179 |
6 | BAA09g65950 | A09 | 60506196 | C | T | upstream_gene_variant | MODIFIER | c.-1459G>A| |
S113 |
7 | BAA09g65950 | A09 | 60506922 | G | A | upstream_gene_variant | MODIFIER | c.-2185C>T| |
S12 |
8 | BAA09g65950 | A09 | 60506937 | C | T | upstream_gene_variant | MODIFIER | c.-2200G>A| |
S140 |
9 | BAA09g65950 | A09 | 60508416 | C | T | upstream_gene_variant | MODIFIER | c.-3679G>A| |
S183 S198 |
10 | BAA09g65950 | A09 | 60508512 | G | A | upstream_gene_variant | MODIFIER | c.-3775C>T| |
S57 |