Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g10140 | A07 | 19016679 | C | T | missense_variant | MODERATE | c.2275G>A|p.Ala759Thr |
S20 |
2 | BAA07g10140 | A07 | 19016799 | C | T | missense_variant | MODERATE | c.2155G>A|p.Glu719Lys |
S96 |
3 | BAA07g10140 | A07 | 19017070 | G | A | synonymous_variant | LOW | c.1884C>T|p.Asp628Asp |
S245 |
4 | BAA07g10140 | A07 | 19017140 | G | A | missense_variant | MODERATE | c.1814C>T|p.Pro605Leu |
S271 |
5 | BAA07g10140 | A07 | 19018679 | C | T | missense_variant | MODERATE | c.1487G>A|p.Cys496Tyr |
S289 S290 |
6 | BAA07g10140 | A07 | 19020494 | C | T | missense_variant | MODERATE | c.701G>A|p.Ser234Asn |
S270 |
7 | BAA07g10140 | A07 | 19020740 | C | T | missense_variant | MODERATE | c.592G>A|p.Val198Met |
S167 |
8 | BAA07g10140 | A07 | 19021266 | C | T | synonymous_variant | LOW | c.453G>A|p.Leu151Leu |
S156 |
9 | BAA07g10140 | A07 | 19022642 | C | T | upstream_gene_variant | MODIFIER | c.-93G>A| |
S256 |
10 | BAA07g10140 | A07 | 19023167 | C | T | upstream_gene_variant | MODIFIER | c.-618G>A| |
S198 |
11 | BAA07g10140 | A07 | 19023565 | C | T | upstream_gene_variant | MODIFIER | c.-1016G>A| |
S86 |