Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02170 | A01 | 1004191 | C | T | missense_variant | MODERATE | c.689G>A|p.Gly230Asp |
S139 |
2 | BAA01g02170 | A01 | 1004643 | G | A | missense_variant | MODERATE | c.344C>T|p.Ala115Val |
S9 |
3 | BAA01g02170 | A01 | 1004689 | C | T | missense_variant | MODERATE | c.298G>A|p.Glu100Lys |
S206 S26 |
4 | BAA01g02170 | A01 | 1004696 | C | T | synonymous_variant | LOW | c.291G>A|p.Glu97Glu |
S305 |
5 | BAA01g02170 | A01 | 1005211 | C | T | upstream_gene_variant | MODIFIER | c.-225G>A| |
S240 |
6 | BAA01g02170 | A01 | 1006199 | C | T | upstream_gene_variant | MODIFIER | c.-1213G>A| |
S291 |
7 | BAA01g02170 | A01 | 1006284 | G | A | upstream_gene_variant | MODIFIER | c.-1298C>T| |
S202 |
8 | BAA01g02170 | A01 | 1006750 | C | T | upstream_gene_variant | MODIFIER | c.-1764G>A| |
S50 |
9 | BAA01g02170 | A01 | 1009031 | C | T | upstream_gene_variant | MODIFIER | c.-4045G>A| |
S50 |