Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g07860 | A05 | 3947415 | G | A | missense_variant | MODERATE | c.2207C>T|p.Ser736Phe |
S272 |
2 | BAA05g07860 | A05 | 3947436 | G | A | missense_variant | MODERATE | c.2186C>T|p.Ser729Phe |
S282 |
3 | BAA05g07860 | A05 | 3947538 | C | T | missense_variant | MODERATE | c.2084G>A|p.Ser695Asn |
S52 |
4 | BAA05g07860 | A05 | 3947725 | G | A | missense_variant | MODERATE | c.1897C>T|p.Pro633Ser |
S78 |
5 | BAA05g07860 | A05 | 3948761 | C | T | missense_variant | MODERATE | c.1273G>A|p.Ala425Thr |
S107 |
6 | BAA05g07860 | A05 | 3949141 | C | T | missense_variant | MODERATE | c.893G>A|p.Arg298Gln |
S203 |
7 | BAA05g07860 | A05 | 3949186 | G | A | missense_variant | MODERATE | c.848C>T|p.Ala283Val |
S272 |
8 | BAA05g07860 | A05 | 3949357 | C | T | stop_gained | HIGH | c.759G>A|p.Trp253* |
S295 |
9 | BAA05g07860 | A05 | 3950209 | G | A | synonymous_variant | LOW | c.297C>T|p.Leu99Leu |
S156 |
10 | BAA05g07860 | A05 | 3950623 | G | A | upstream_gene_variant | MODIFIER | c.-118C>T| |
S39 |
11 | BAA05g07860 | A05 | 3951009 | G | A | upstream_gene_variant | MODIFIER | c.-504C>T| |
S38 |
12 | BAA05g07860 | A05 | 3953311 | C | T | upstream_gene_variant | MODIFIER | c.-2806G>A| |
S236 |
13 | BAA05g07860 | A05 | 3954487 | G | A | upstream_gene_variant | MODIFIER | c.-3982C>T| |
S134 |