Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g03930 | A03 | 1685372 | G | A | synonymous_variant | LOW | c.1122C>T|p.Thr374Thr |
S275 |
2 | BAA03g03930 | A03 | 1686083 | G | A | synonymous_variant | LOW | c.681C>T|p.Leu227Leu |
S75 S81 |
3 | BAA03g03930 | A03 | 1686131 | C | A | splice_acceptor_variant&intron_variant | HIGH | c.634-1G>T| |
S299 |
4 | BAA03g03930 | A03 | 1686864 | C | T | missense_variant | MODERATE | c.265G>A|p.Gly89Ser |
S259 |
5 | BAA03g03930 | A03 | 1686939 | G | A | missense_variant | MODERATE | c.190C>T|p.Pro64Ser |
S188 |
6 | BAA03g03930 | A03 | 1687049 | G | A | missense_variant | MODERATE | c.80C>T|p.Pro27Leu |
S78 S83 |
7 | BAA03g03930 | A03 | 1688817 | A | T | upstream_gene_variant | MODIFIER | c.-1689T>A| |
S61 |
8 | BAA03g03930 | A03 | 1690197 | C | T | upstream_gene_variant | MODIFIER | c.-3069G>A| |
S134 |
9 | BAA03g03930 | A03 | 1690489 | G | A | upstream_gene_variant | MODIFIER | c.-3361C>T| |
S166 S167 S257 |
10 | BAA03g03930 | A03 | 1690616 | G | A | upstream_gene_variant | MODIFIER | c.-3488C>T| |
S278 |
11 | BAA03g03930 | A03 | 1690973 | G | A | upstream_gene_variant | MODIFIER | c.-3845C>T| |
S149 |