Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19460 | A09 | 11892355 | G | A | upstream_gene_variant | MODIFIER | c.-4839G>A| |
S55 |
2 | BAA09g19460 | A09 | 11893624 | G | A | upstream_gene_variant | MODIFIER | c.-3570G>A| |
S211 |
3 | BAA09g19460 | A09 | 11896724 | C | T | upstream_gene_variant | MODIFIER | c.-470C>T| |
S241 |
4 | BAA09g19460 | A09 | 11897221 | G | A | missense_variant | MODERATE | c.28G>A|p.Ala10Thr |
S236 |
5 | BAA09g19460 | A09 | 11897800 | G | A | missense_variant | MODERATE | c.217G>A|p.Gly73Ser |
S182 |
6 | BAA09g19460 | A09 | 11898957 | G | A | missense_variant | MODERATE | c.1007G>A|p.Gly336Asp |
S47 |
7 | BAA09g19460 | A09 | 11898994 | A | C | splice_region_variant&intron_variant | LOW | c.1041+3A>C| |
S224 S271 S272 |
8 | BAA09g19460 | A09 | 11899446 | C | T | missense_variant | MODERATE | c.1330C>T|p.Pro444Ser |
S148 S210 |
9 | BAA09g19460 | A09 | 11902358 | G | A | downstream_gene_variant | MODIFIER | c.*1538G>A| |
S288 |
10 | BAA09g19460 | A09 | 11902546 | C | T | downstream_gene_variant | MODIFIER | c.*1726C>T| |
S64 |