Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g16120 | A06 | 8041711 | C | T | missense_variant | MODERATE | c.670G>A|p.Glu224Lys |
S308 |
2 | BAA06g16120 | A06 | 8041900 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.565-1G>A| |
S279 |
3 | BAA06g16120 | A06 | 8042906 | G | A | missense_variant | MODERATE | c.202C>T|p.Pro68Ser |
S182 |
4 | BAA06g16120 | A06 | 8042941 | C | T | missense_variant | MODERATE | c.167G>A|p.Gly56Glu |
S189 |
5 | BAA06g16120 | A06 | 8042999 | G | A | stop_gained | HIGH | c.109C>T|p.Gln37* |
S292 |
6 | BAA06g16120 | A06 | 8044510 | G | A | upstream_gene_variant | MODIFIER | c.-1403C>T| |
S295 |
7 | BAA06g16120 | A06 | 8044834 | G | A | upstream_gene_variant | MODIFIER | c.-1727C>T| |
S159 S187 S188 S243 S276 |
8 | BAA06g16120 | A06 | 8046299 | C | T | upstream_gene_variant | MODIFIER | c.-3192G>A| |
S271 |
9 | BAA06g16120 | A06 | 8046503 | G | A | upstream_gene_variant | MODIFIER | c.-3396C>T| |
S177 |
10 | BAA06g16120 | A06 | 8046651 | C | T | upstream_gene_variant | MODIFIER | c.-3544G>A| |
S114 |
11 | BAA06g16120 | A06 | 8047068 | C | T | upstream_gene_variant | MODIFIER | c.-3961G>A| |
S205 |
12 | BAA06g16120 | A06 | 8047695 | C | T | upstream_gene_variant | MODIFIER | c.-4588G>A| |
S11 |