| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g10260 | A02 | 4562244 | C | T | missense_variant | MODERATE | c.1168G>A|p.Val390Ile |
S288 |
| 2 | BAA02g10260 | A02 | 4562527 | G | A | synonymous_variant | LOW | c.957C>T|p.Phe319Phe |
S169 |
| 3 | BAA02g10260 | A02 | 4562862 | C | T | missense_variant | MODERATE | c.622G>A|p.Asp208Asn |
S301 S304 |
| 4 | BAA02g10260 | A02 | 4563809 | G | A | synonymous_variant | LOW | c.51C>T|p.Phe17Phe |
S210 |
| 5 | BAA02g10260 | A02 | 4567421 | G | A | upstream_gene_variant | MODIFIER | c.-3494C>T| |
S231 S9 |
| 6 | BAA02g10260 | A02 | 4567920 | C | T | upstream_gene_variant | MODIFIER | c.-3993G>A| |
S15 S3 |