Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g37860 | A07 | 34696023 | C | T | missense_variant | MODERATE | c.2596G>A|p.Gly866Arg |
S234 |
2 | BAA07g37860 | A07 | 34696622 | G | A | missense_variant | MODERATE | c.2158C>T|p.Pro720Ser |
S263 |
3 | BAA07g37860 | A07 | 34697357 | C | T | missense_variant | MODERATE | c.1486G>A|p.Glu496Lys |
S158 |
4 | BAA07g37860 | A07 | 34697543 | C | T | missense_variant | MODERATE | c.1375G>A|p.Glu459Lys |
S47 |
5 | BAA07g37860 | A07 | 34697987 | C | T | missense_variant | MODERATE | c.1001G>A|p.Gly334Glu |
S114 |
6 | BAA07g37860 | A07 | 34698285 | C | T | missense_variant | MODERATE | c.774G>A|p.Met258Ile |
S95 |
7 | BAA07g37860 | A07 | 34698702 | C | T | synonymous_variant | LOW | c.507G>A|p.Lys169Lys |
S266 |
8 | BAA07g37860 | A07 | 34698906 | G | A | missense_variant | MODERATE | c.370C>T|p.Leu124Phe |
S40 S49 |
9 | BAA07g37860 | A07 | 34699360 | G | A | missense_variant | MODERATE | c.107C>T|p.Ala36Val |
S283 |
10 | BAA07g37860 | A07 | 34699966 | C | T | upstream_gene_variant | MODIFIER | c.-500G>A| |
S239 S33 |
11 | BAA07g37860 | A07 | 34701454 | G | A | upstream_gene_variant | MODIFIER | c.-1988C>T| |
S171 |
12 | BAA07g37860 | A07 | 34704152 | C | T | upstream_gene_variant | MODIFIER | c.-4686G>A| |
S296 |