Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g25400 | A05 | 30239948 | C | T | upstream_gene_variant | MODIFIER | c.-4532C>T| |
S132 S137 S215 S237 |
2 | BAA05g25400 | A05 | 30240000 | G | A | upstream_gene_variant | MODIFIER | c.-4480G>A| |
S158 |
3 | BAA05g25400 | A05 | 30240076 | G | A | upstream_gene_variant | MODIFIER | c.-4404G>A| |
S185 |
4 | BAA05g25400 | A05 | 30240191 | C | T | upstream_gene_variant | MODIFIER | c.-4289C>T| |
S277 |
5 | BAA05g25400 | A05 | 30240286 | G | A | upstream_gene_variant | MODIFIER | c.-4194G>A| |
S90 |
6 | BAA05g25400 | A05 | 30244552 | G | A | missense_variant | MODERATE | c.73G>A|p.Glu25Lys |
S243 S299 |
7 | BAA05g25400 | A05 | 30244711 | G | A | missense_variant | MODERATE | c.232G>A|p.Asp78Asn |
S103 |
8 | BAA05g25400 | A05 | 30244805 | C | T | missense_variant | MODERATE | c.326C>T|p.Pro109Leu |
S116 |
9 | BAA05g25400 | A05 | 30244861 | C | T | missense_variant | MODERATE | c.382C>T|p.Pro128Ser |
S193 |