Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19480 | A02 | 10105070 | G | A | missense_variant | MODERATE | c.368C>T|p.Ser123Phe |
S297 |
2 | BAA02g19480 | A02 | 10105278 | G | A | missense_variant | MODERATE | c.160C>T|p.Pro54Ser |
S61 |
3 | BAA02g19480 | A02 | 10105984 | C | T | upstream_gene_variant | MODIFIER | c.-547G>A| |
S88 |
4 | BAA02g19480 | A02 | 10106708 | G | A | upstream_gene_variant | MODIFIER | c.-1271C>T| |
S137 S215 |
5 | BAA02g19480 | A02 | 10107059 | C | T | upstream_gene_variant | MODIFIER | c.-1622G>A| |
S180 |
6 | BAA02g19480 | A02 | 10108158 | G | A | upstream_gene_variant | MODIFIER | c.-2721C>T| |
S41 |
7 | BAA02g19480 | A02 | 10109696 | C | T | upstream_gene_variant | MODIFIER | c.-4259G>A| |
S80 |