Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g25190 | A03 | 11539403 | C | T | upstream_gene_variant | MODIFIER | c.-4447C>T| |
S82 S92 |
2 | BAA03g25190 | A03 | 11540997 | G | A | upstream_gene_variant | MODIFIER | c.-2853G>A| |
S44 |
3 | BAA03g25190 | A03 | 11544175 | G | A | missense_variant | MODERATE | c.326G>A|p.Gly109Glu |
S255 |
4 | BAA03g25190 | A03 | 11544351 | G | A | missense_variant | MODERATE | c.502G>A|p.Ala168Thr |
S51 |
5 | BAA03g25190 | A03 | 11544847 | G | A | missense_variant | MODERATE | c.998G>A|p.Gly333Glu |
S33 |
6 | BAA03g25190 | A03 | 11544975 | C | T | synonymous_variant | LOW | c.1126C>T|p.Leu376Leu |
S252 |
7 | BAA03g25190 | A03 | 11545391 | C | T | synonymous_variant | LOW | c.1542C>T|p.Leu514Leu |
S16 |
8 | BAA03g25190 | A03 | 11545991 | G | A | synonymous_variant | LOW | c.2142G>A|p.Gln714Gln |
S183 |
9 | BAA03g25190 | A03 | 11546272 | C | T | missense_variant | MODERATE | c.2423C>T|p.Ala808Val |
S221 S59 |
10 | BAA03g25190 | A03 | 11546293 | C | T | missense_variant | MODERATE | c.2444C>T|p.Ser815Phe |
S153 |
11 | BAA03g25190 | A03 | 11547074 | C | T | downstream_gene_variant | MODIFIER | c.*693C>T| |
S255 |