Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02110 | A01 | 969211 | C | T | missense_variant | MODERATE | c.1303G>A|p.Glu435Lys |
S8 |
2 | BAA01g02110 | A01 | 969292 | C | T | missense_variant | MODERATE | c.1222G>A|p.Asp408Asn |
S255 |
3 | BAA01g02110 | A01 | 969327 | C | T | missense_variant | MODERATE | c.1187G>A|p.Cys396Tyr |
S189 |
4 | BAA01g02110 | A01 | 969546 | C | T | missense_variant | MODERATE | c.968G>A|p.Gly323Glu |
S75 S81 |
5 | BAA01g02110 | A01 | 969695 | C | T | synonymous_variant | LOW | c.819G>A|p.Lys273Lys |
S117 |
6 | BAA01g02110 | A01 | 971343 | C | T | upstream_gene_variant | MODIFIER | c.-542G>A| |
S25 |
7 | BAA01g02110 | A01 | 973005 | G | A | upstream_gene_variant | MODIFIER | c.-2204C>T| |
S15 S3 |
8 | BAA01g02110 | A01 | 973460 | G | A | upstream_gene_variant | MODIFIER | c.-2659C>T| |
S293 |
9 | BAA01g02110 | A01 | 974425 | C | T | upstream_gene_variant | MODIFIER | c.-3624G>A| |
S113 |