| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g08850 | A08 | 8054826 | C | T | missense_variant | MODERATE | c.1367G>A|p.Arg456Lys |
S152 |
| 2 | BAA08g08850 | A08 | 8056370 | C | T | synonymous_variant | LOW | c.537G>A|p.Lys179Lys |
S278 |
| 3 | BAA08g08850 | A08 | 8056426 | C | T | splice_region_variant&intron_variant | LOW | c.488-7G>A| |
S126 |
| 4 | BAA08g08850 | A08 | 8056479 | G | A | splice_region_variant&intron_variant | LOW | c.487+6C>T| |
S164 |
| 5 | BAA08g08850 | A08 | 8056949 | A | C | missense_variant | MODERATE | c.23T>G|p.Leu8Arg |
S138 |
| 6 | BAA08g08850 | A08 | 8059894 | C | T | upstream_gene_variant | MODIFIER | c.-2923G>A| |
S2 |
| 7 | BAA08g08850 | A08 | 8060293 | C | T | upstream_gene_variant | MODIFIER | c.-3322G>A| |
S67 |
| 8 | BAA08g08850 | A08 | 8061733 | C | T | upstream_gene_variant | MODIFIER | c.-4762G>A| |
S209 |