Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05930 | A01 | 2655356 | G | A | missense_variant | MODERATE | c.2362C>T|p.Pro788Ser |
S5 |
2 | BAA01g05930 | A01 | 2656817 | C | T | synonymous_variant | LOW | c.1380G>A|p.Gln460Gln |
S50 |
3 | BAA01g05930 | A01 | 2657887 | C | T | splice_donor_variant&intron_variant | HIGH | c.818+1G>A| |
S132 S137 S215 S89 |
4 | BAA01g05930 | A01 | 2658146 | G | A | missense_variant | MODERATE | c.644C>T|p.Pro215Leu |
S209 |
5 | BAA01g05930 | A01 | 2658366 | G | A | stop_gained | HIGH | c.424C>T|p.Gln142* |
S32 |
6 | BAA01g05930 | A01 | 2659990 | G | A | upstream_gene_variant | MODIFIER | c.-165C>T| |
S14 S224 |
7 | BAA01g05930 | A01 | 2659997 | G | A | upstream_gene_variant | MODIFIER | c.-172C>T| |
S204 |
8 | BAA01g05930 | A01 | 2660594 | C | T | upstream_gene_variant | MODIFIER | c.-769G>A| |
S269 |
9 | BAA01g05930 | A01 | 2660637 | G | A | upstream_gene_variant | MODIFIER | c.-812C>T| |
S162 |
10 | BAA01g05930 | A01 | 2660791 | G | A | upstream_gene_variant | MODIFIER | c.-966C>T| |
S259 |
11 | BAA01g05930 | A01 | 2660845 | G | A | upstream_gene_variant | MODIFIER | c.-1020C>T| |
S204 |
12 | BAA01g05930 | A01 | 2661012 | G | A | upstream_gene_variant | MODIFIER | c.-1187C>T| |
S262 |
13 | BAA01g05930 | A01 | 2661651 | G | A | upstream_gene_variant | MODIFIER | c.-1826C>T| |
S190 |
14 | BAA01g05930 | A01 | 2662742 | G | A | upstream_gene_variant | MODIFIER | c.-2917C>T| |
S286 |
15 | BAA01g05930 | A01 | 2664600 | C | T | upstream_gene_variant | MODIFIER | c.-4775G>A| |
S125 |