| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g02670 | A01 | 1218099 | G | A | downstream_gene_variant | MODIFIER | c.*3647C>T| |
S298 |
| 2 | BAA01g02670 | A01 | 1218408 | G | A | downstream_gene_variant | MODIFIER | c.*3338C>T| |
S23 |
| 3 | BAA01g02670 | A01 | 1221793 | C | T | missense_variant | MODERATE | c.1408G>A|p.Asp470Asn |
S230 |
| 4 | BAA01g02670 | A01 | 1222544 | C | T | missense_variant | MODERATE | c.970G>A|p.Ala324Thr |
S38 |
| 5 | BAA01g02670 | A01 | 1223347 | G | A | missense_variant | MODERATE | c.496C>T|p.Pro166Ser |
S202 S256 |
| 6 | BAA01g02670 | A01 | 1228548 | C | T | upstream_gene_variant | MODIFIER | c.-4462G>A| |
S132 S137 S215 |
| 7 | BAA01g02670 | A01 | 1228947 | G | A | upstream_gene_variant | MODIFIER | c.-4861C>T| |
S123 |
| 8 | BAA01g02670 | A01 | 1228967 | A | C | upstream_gene_variant | MODIFIER | c.-4881T>G| |
S206 |
| 9 | BAA01g02670 | A01 | 1228999 | C | T | upstream_gene_variant | MODIFIER | c.-4913G>A| |
S148 S210 |