Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21050 | A01 | 10355627 | G | A | missense_variant | MODERATE | c.994C>T|p.Leu332Phe |
S263 |
2 | BAA01g21050 | A01 | 10355771 | G | A | synonymous_variant | LOW | c.850C>T|p.Leu284Leu |
S163 |
3 | BAA01g21050 | A01 | 10361610 | C | T | missense_variant | MODERATE | c.652G>A|p.Glu218Lys |
S25 S264 |
4 | BAA01g21050 | A01 | 10362621 | C | T | synonymous_variant | LOW | c.45G>A|p.Glu15Glu |
S4 |
5 | BAA01g21050 | A01 | 10363804 | G | A | upstream_gene_variant | MODIFIER | c.-1139C>T| |
S228 |
6 | BAA01g21050 | A01 | 10364121 | C | T | upstream_gene_variant | MODIFIER | c.-1456G>A| |
S164 |
7 | BAA01g21050 | A01 | 10366753 | G | A | upstream_gene_variant | MODIFIER | c.-4088C>T| |
S302 |