Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47090 | A02 | 38079441 | C | T | missense_variant | MODERATE | c.380G>A|p.Gly127Asp |
S52 |
2 | BAA02g47090 | A02 | 38079579 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.243-1G>A| |
S194 |
3 | BAA02g47090 | A02 | 38081102 | G | A | upstream_gene_variant | MODIFIER | c.-717C>T| |
S164 |
4 | BAA02g47090 | A02 | 38081969 | G | A | upstream_gene_variant | MODIFIER | c.-1584C>T| |
S281 |
5 | BAA02g47090 | A02 | 38082340 | C | T | upstream_gene_variant | MODIFIER | c.-1955G>A| |
S167 |
6 | BAA02g47090 | A02 | 38082765 | G | A | upstream_gene_variant | MODIFIER | c.-2380C>T| |
S113 |
7 | BAA02g47090 | A02 | 38082857 | C | T | upstream_gene_variant | MODIFIER | c.-2472G>A| |
S98 |
8 | BAA02g47090 | A02 | 38083724 | C | T | upstream_gene_variant | MODIFIER | c.-3339G>A| |
S158 |