Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22440 | A09 | 14035217 | C | T | missense_variant | MODERATE | c.28C>T|p.Pro10Ser |
S193 |
2 | BAA09g22440 | A09 | 14035612 | G | A | synonymous_variant | LOW | c.423G>A|p.Glu141Glu |
S40 S49 |
3 | BAA09g22440 | A09 | 14036245 | G | A | missense_variant | MODERATE | c.964G>A|p.Asp322Asn |
S46 |
4 | BAA09g22440 | A09 | 14036632 | G | A | missense_variant | MODERATE | c.1351G>A|p.Glu451Lys |
S78 S83 |
5 | BAA09g22440 | A09 | 14038416 | C | T | synonymous_variant | LOW | c.2892C>T|p.Cys964Cys |
S2 |
6 | BAA09g22440 | A09 | 14038770 | C | T | synonymous_variant | LOW | c.3246C>T|p.Ser1082Ser |
S234 |
7 | BAA09g22440 | A09 | 14039336 | G | A | downstream_gene_variant | MODIFIER | c.*215G>A| |
S28 |
8 | BAA09g22440 | A09 | 14039479 | G | A | downstream_gene_variant | MODIFIER | c.*358G>A| |
S45 |
9 | BAA09g22440 | A09 | 14040133 | C | T | downstream_gene_variant | MODIFIER | c.*1012C>T| |
S36 |