Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26660 | A01 | 14966198 | C | T | missense_variant | MODERATE | c.215G>A|p.Arg72Lys |
S170 |
2 | BAA01g26660 | A01 | 14966427 | G | A | missense_variant | MODERATE | c.80C>T|p.Ala27Val |
S33 |
3 | BAA01g26660 | A01 | 14966756 | G | A | upstream_gene_variant | MODIFIER | c.-250C>T| |
S5 |
4 | BAA01g26660 | A01 | 14967125 | C | T | upstream_gene_variant | MODIFIER | c.-619G>A| |
S42 |
5 | BAA01g26660 | A01 | 14967794 | G | A | upstream_gene_variant | MODIFIER | c.-1288C>T| |
S110 S13 S219 S279 S72 |
6 | BAA01g26660 | A01 | 14968703 | G | A | upstream_gene_variant | MODIFIER | c.-2197C>T| |
S301 S304 |
7 | BAA01g26660 | A01 | 14968742 | C | T | upstream_gene_variant | MODIFIER | c.-2236G>A| |
S151 |
8 | BAA01g26660 | A01 | 14969114 | G | A | upstream_gene_variant | MODIFIER | c.-2608C>T| |
S37 |
9 | BAA01g26660 | A01 | 14969401 | G | A | upstream_gene_variant | MODIFIER | c.-2895C>T| |
S262 |
10 | BAA01g26660 | A01 | 14970562 | C | T | upstream_gene_variant | MODIFIER | c.-4056G>A| |
S183 |
11 | BAA01g26660 | A01 | 14970565 | C | T | upstream_gene_variant | MODIFIER | c.-4059G>A| |
S230 |
12 | BAA01g26660 | A01 | 14971170 | G | A | upstream_gene_variant | MODIFIER | c.-4664C>T| |
S172 S217 |
13 | BAA01g26660 | A01 | 14971182 | C | T | upstream_gene_variant | MODIFIER | c.-4676G>A| |
S235 |