| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g02050 | A01 | 948652 | G | A | missense_variant | MODERATE | c.1714C>T|p.Pro572Ser |
S239 |
| 2 | BAA01g02050 | A01 | 949223 | C | T | stop_gained | HIGH | c.1143G>A|p.Trp381* |
S119 |
| 3 | BAA01g02050 | A01 | 949760 | C | T | synonymous_variant | LOW | c.606G>A|p.Gln202Gln |
S69 |
| 4 | BAA01g02050 | A01 | 950036 | G | A | synonymous_variant | LOW | c.330C>T|p.Val110Val |
S162 |
| 5 | BAA01g02050 | A01 | 950091 | C | T | missense_variant | MODERATE | c.275G>A|p.Arg92His |
S76 |
| 6 | BAA01g02050 | A01 | 953467 | G | A | upstream_gene_variant | MODIFIER | c.-3102C>T| |
S191 |
| 7 | BAA01g02050 | A01 | 954088 | C | T | upstream_gene_variant | MODIFIER | c.-3723G>A| |
S40 S49 |
| 8 | BAA01g02050 | A01 | 955123 | G | A | upstream_gene_variant | MODIFIER | c.-4758C>T| |
S295 |