Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g34060 | A10 | 24064767 | G | A | missense_variant | MODERATE | c.601C>T|p.Arg201Cys |
S62 |
2 | BAA10g34060 | A10 | 24064941 | C | T | missense_variant | MODERATE | c.427G>A|p.Val143Met |
S72 |
3 | BAA10g34060 | A10 | 24065000 | G | A | missense_variant | MODERATE | c.368C>T|p.Pro123Leu |
S183 S198 |
4 | BAA10g34060 | A10 | 24065055 | C | T | missense_variant | MODERATE | c.313G>A|p.Ala105Thr |
S92 |
5 | BAA10g34060 | A10 | 24065134 | C | T | synonymous_variant | LOW | c.234G>A|p.Ala78Ala |
S200 |
6 | BAA10g34060 | A10 | 24066991 | C | T | upstream_gene_variant | MODIFIER | c.-1624G>A| |
S210 |
7 | BAA10g34060 | A10 | 24069031 | A | G | upstream_gene_variant | MODIFIER | c.-3664T>C| |
S108 S119 S157 S161 S174 S182 S186 S198 S200 S209 S212 S247 S286 S293 S56 S64 S84 S94 |
8 | BAA10g34060 | A10 | 24069693 | C | T | upstream_gene_variant | MODIFIER | c.-4326G>A| |
S100 |