| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g11350 | A08 | 10107975 | G | A | missense_variant | MODERATE | c.755C>T|p.Ala252Val |
S32 |
| 2 | BAA08g11350 | A08 | 10107992 | C | T | synonymous_variant | LOW | c.738G>A|p.Lys246Lys |
S36 |
| 3 | BAA08g11350 | A08 | 10108019 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.712-1G>A| |
S6 |
| 4 | BAA08g11350 | A08 | 10108219 | C | T | missense_variant | MODERATE | c.583G>A|p.Glu195Lys |
S51 |
| 5 | BAA08g11350 | A08 | 10108383 | C | T | missense_variant&splice_region_variant | MODERATE | c.470G>A|p.Gly157Glu |
S15 S3 |
| 6 | BAA08g11350 | A08 | 10109859 | G | A | upstream_gene_variant | MODIFIER | c.-42C>T| |
S195 |
| 7 | BAA08g11350 | A08 | 10111605 | C | T | upstream_gene_variant | MODIFIER | c.-1788G>A| |
S148 S210 S30 S31 |
| 8 | BAA08g11350 | A08 | 10112745 | G | A | upstream_gene_variant | MODIFIER | c.-2928C>T| |
S286 |