Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g30660 | A08 | 20643938 | C | T | missense_variant | MODERATE | c.1415G>A|p.Gly472Glu |
S250 |
2 | BAA08g30660 | A08 | 20644825 | C | T | missense_variant | MODERATE | c.938G>A|p.Gly313Asp |
S159 S243 |
3 | BAA08g30660 | A08 | 20645244 | C | T | missense_variant | MODERATE | c.710G>A|p.Gly237Glu |
S262 |
4 | BAA08g30660 | A08 | 20645819 | G | A | missense_variant | MODERATE | c.335C>T|p.Thr112Ile |
S275 |
5 | BAA08g30660 | A08 | 20645993 | C | T | missense_variant | MODERATE | c.247G>A|p.Gly83Arg |
S65 |
6 | BAA08g30660 | A08 | 20649122 | C | T | upstream_gene_variant | MODIFIER | c.-2720G>A| |
S173 |
7 | BAA08g30660 | A08 | 20649375 | C | T | upstream_gene_variant | MODIFIER | c.-2973G>A| |
S294 |
8 | BAA08g30660 | A08 | 20650233 | C | T | upstream_gene_variant | MODIFIER | c.-3831G>A| |
S153 |