Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01780 | A10 | 850389 | C | T | missense_variant | MODERATE | c.116G>A|p.Gly39Glu |
S79 S91 |
2 | BAA10g01780 | A10 | 850647 | G | A | upstream_gene_variant | MODIFIER | c.-143C>T| |
S303 |
3 | BAA10g01780 | A10 | 851084 | C | T | upstream_gene_variant | MODIFIER | c.-580G>A| |
S122 |
4 | BAA10g01780 | A10 | 851318 | G | A | upstream_gene_variant | MODIFIER | c.-814C>T| |
S66 |
5 | BAA10g01780 | A10 | 851490 | C | T | upstream_gene_variant | MODIFIER | c.-986G>A| |
S163 |
6 | BAA10g01780 | A10 | 855489 | C | T | upstream_gene_variant | MODIFIER | c.-4985G>A| |
S188 |