| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g10820 | A08 | 9721742 | G | A | upstream_gene_variant | MODIFIER | c.-657G>A| |
S223 |
| 2 | BAA08g10820 | A08 | 9722561 | G | A | missense_variant | MODERATE | c.163G>A|p.Ala55Thr |
S297 |
| 3 | BAA08g10820 | A08 | 9724196 | G | A | synonymous_variant | LOW | c.1386G>A|p.Val462Val |
S263 |
| 4 | BAA08g10820 | A08 | 9726158 | C | T | intron_variant | MODIFIER | c.2290-9C>T| |
S50 |
| 5 | BAA08g10820 | A08 | 9726317 | G | A | intron_variant | MODIFIER | c.2393+47G>A| |
S245 |
| 6 | BAA08g10820 | A08 | 9726545 | G | A | missense_variant | MODERATE | c.2530G>A|p.Asp844Asn |
S174 |
| 7 | BAA08g10820 | A08 | 9727473 | C | T | missense_variant | MODERATE | c.3109C>T|p.Pro1037Ser |
S36 |
| 8 | BAA08g10820 | A08 | 9729222 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.4064-1G>A| |
S136 |
| 9 | BAA08g10820 | A08 | 9729329 | G | A | intron_variant | MODIFIER | c.4120-27G>A| |
S260 |