| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g13250 | A05 | 6857065 | C | T | missense_variant | MODERATE | c.119C>T|p.Pro40Leu |
S15 S3 |
| 2 | BAA05g13250 | A05 | 6857754 | G | A | intron_variant | MODIFIER | c.453+59G>A| |
S25 S264 |
| 3 | BAA05g13250 | A05 | 6858059 | G | A | missense_variant | MODERATE | c.599G>A|p.Arg200Lys |
S260 |
| 4 | BAA05g13250 | A05 | 6858079 | G | A | missense_variant | MODERATE | c.619G>A|p.Gly207Ser |
S6 |
| 5 | BAA05g13250 | A05 | 6858125 | C | T | missense_variant | MODERATE | c.665C>T|p.Thr222Ile |
S267 |
| 6 | BAA05g13250 | A05 | 6858308 | G | A | splice_donor_variant&intron_variant | HIGH | c.774+1G>A| |
S243 S299 |
| 7 | BAA05g13250 | A05 | 6859176 | C | T | intron_variant | MODIFIER | c.1140+20C>T| |
S136 |
| 8 | BAA05g13250 | A05 | 6861013 | G | A | downstream_gene_variant | MODIFIER | c.*1408G>A| |
S8 |
| 9 | BAA05g13250 | A05 | 6861237 | C | T | downstream_gene_variant | MODIFIER | c.*1632C>T| |
S175 |