Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g30110 | A08 | 20470084 | C | T | missense_variant | MODERATE | c.1777G>A|p.Ala593Thr |
S262 |
2 | BAA08g30110 | A08 | 20470962 | C | T | missense_variant | MODERATE | c.1367G>A|p.Gly456Glu |
S262 |
3 | BAA08g30110 | A08 | 20471126 | C | T | synonymous_variant | LOW | c.1203G>A|p.Ala401Ala |
S189 |
4 | BAA08g30110 | A08 | 20471846 | C | T | missense_variant | MODERATE | c.805G>A|p.Asp269Asn |
S63 |
5 | BAA08g30110 | A08 | 20472384 | C | T | missense_variant | MODERATE | c.439G>A|p.Asp147Asn |
S198 |
6 | BAA08g30110 | A08 | 20475356 | C | T | upstream_gene_variant | MODIFIER | c.-2121G>A| |
S228 |
7 | BAA08g30110 | A08 | 20476005 | C | T | upstream_gene_variant | MODIFIER | c.-2770G>A| |
S133 |
8 | BAA08g30110 | A08 | 20477457 | G | A | upstream_gene_variant | MODIFIER | c.-4222C>T| |
S229 |