Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g26660 | A03 | 12264811 | C | T | missense_variant | MODERATE | c.1321G>A|p.Gly441Arg |
S59 |
2 | BAA03g26660 | A03 | 12264899 | C | T | synonymous_variant | LOW | c.1233G>A|p.Thr411Thr |
S158 |
3 | BAA03g26660 | A03 | 12265118 | C | T | stop_gained | HIGH | c.1014G>A|p.Trp338* |
S192 |
4 | BAA03g26660 | A03 | 12265666 | G | A | missense_variant | MODERATE | c.620C>T|p.Thr207Met |
S164 |
5 | BAA03g26660 | A03 | 12266938 | C | T | upstream_gene_variant | MODIFIER | c.-406G>A| |
S134 |
6 | BAA03g26660 | A03 | 12267744 | G | A | upstream_gene_variant | MODIFIER | c.-1212C>T| |
S128 S96 |
7 | BAA03g26660 | A03 | 12268024 | G | A | upstream_gene_variant | MODIFIER | c.-1492C>T| |
S206 S26 |
8 | BAA03g26660 | A03 | 12269439 | C | T | upstream_gene_variant | MODIFIER | c.-2907G>A| |
S32 |