Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44020 | A09 | 49897803 | C | T | missense_variant | MODERATE | c.1613G>A|p.Gly538Glu |
S168 |
2 | BAA09g44020 | A09 | 49897809 | C | T | missense_variant | MODERATE | c.1607G>A|p.Arg536Gln |
S157 |
3 | BAA09g44020 | A09 | 49898695 | G | A | missense_variant | MODERATE | c.1186C>T|p.Pro396Ser |
S157 |
4 | BAA09g44020 | A09 | 49899959 | C | T | synonymous_variant | LOW | c.591G>A|p.Arg197Arg |
S301 S304 |
5 | BAA09g44020 | A09 | 49900102 | C | T | missense_variant | MODERATE | c.570G>A|p.Met190Ile |
S278 |
6 | BAA09g44020 | A09 | 49900112 | C | T | stop_gained | HIGH | c.560G>A|p.Trp187* |
S87 |
7 | BAA09g44020 | A09 | 49900661 | C | T | missense_variant | MODERATE | c.199G>A|p.Glu67Lys |
S168 |
8 | BAA09g44020 | A09 | 49904525 | C | T | upstream_gene_variant | MODIFIER | c.-3473G>A| |
S232 |
9 | BAA09g44020 | A09 | 49905335 | G | A | upstream_gene_variant | MODIFIER | c.-4283C>T| |
S71 |
10 | BAA09g44020 | A09 | 49905799 | C | T | upstream_gene_variant | MODIFIER | c.-4747G>A| |
S286 |
11 | BAA09g44020 | A09 | 49905982 | C | T | upstream_gene_variant | MODIFIER | c.-4930G>A| |
S138 |