Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g11600 | A03 | 4792387 | G | A | synonymous_variant | LOW | c.1908C>T|p.Asn636Asn |
S286 |
2 | BAA03g11600 | A03 | 4792554 | G | A | splice_region_variant&intron_variant | LOW | c.1748-7C>T| |
S177 |
3 | BAA03g11600 | A03 | 4792637 | G | A | missense_variant | MODERATE | c.1733C>T|p.Ser578Phe |
S135 |
4 | BAA03g11600 | A03 | 4792823 | G | A | missense_variant | MODERATE | c.1547C>T|p.Ala516Val |
S135 S152 S185 S203 |
5 | BAA03g11600 | A03 | 4792880 | C | T | missense_variant | MODERATE | c.1490G>A|p.Gly497Glu |
S177 |
6 | BAA03g11600 | A03 | 4793484 | G | A | synonymous_variant | LOW | c.963C>T|p.Cys321Cys |
S224 |
7 | BAA03g11600 | A03 | 4794917 | G | A | synonymous_variant | LOW | c.90C>T|p.Pro30Pro |
S286 |
8 | BAA03g11600 | A03 | 4796955 | G | A | upstream_gene_variant | MODIFIER | c.-1949C>T| |
S11 |
9 | BAA03g11600 | A03 | 4797982 | G | A | upstream_gene_variant | MODIFIER | c.-2976C>T| |
S291 |