Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44610 | A01 | 29701491 | C | T | missense_variant | MODERATE | c.532G>A|p.Glu178Lys |
S45 |
2 | BAA01g44610 | A01 | 29701525 | C | T | synonymous_variant | LOW | c.498G>A|p.Ser166Ser |
S132 S215 |
3 | BAA01g44610 | A01 | 29701620 | G | A | missense_variant | MODERATE | c.403C>T|p.Pro135Ser |
S5 |
4 | BAA01g44610 | A01 | 29701786 | G | A | synonymous_variant | LOW | c.237C>T|p.Phe79Phe |
S189 |
5 | BAA01g44610 | A01 | 29701989 | G | A | missense_variant | MODERATE | c.34C>T|p.Pro12Ser |
S265 |
6 | BAA01g44610 | A01 | 29702003 | G | A | missense_variant | MODERATE | c.20C>T|p.Ser7Leu |
S241 |
7 | BAA01g44610 | A01 | 29702354 | G | A | upstream_gene_variant | MODIFIER | c.-332C>T| |
S42 |
8 | BAA01g44610 | A01 | 29705428 | C | T | upstream_gene_variant | MODIFIER | c.-3406G>A| |
S32 |
9 | BAA01g44610 | A01 | 29706159 | C | T | upstream_gene_variant | MODIFIER | c.-4137G>A| |
S242 |