Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35340 | A02 | 30379568 | G | A | upstream_gene_variant | MODIFIER | c.-3027G>A| |
S197 |
2 | BAA02g35340 | A02 | 30380553 | C | T | upstream_gene_variant | MODIFIER | c.-2042C>T| |
S167 |
3 | BAA02g35340 | A02 | 30382538 | C | T | upstream_gene_variant | MODIFIER | c.-57C>T| |
S112 |
4 | BAA02g35340 | A02 | 30382749 | G | A | intron_variant | MODIFIER | c.3+152G>A| |
S153 S213 |
5 | BAA02g35340 | A02 | 30383026 | G | A | intron_variant | MODIFIER | c.4-87G>A| |
S34 |
6 | BAA02g35340 | A02 | 30383158 | G | A | missense_variant | MODERATE | c.49G>A|p.Glu17Lys |
S228 |
7 | BAA02g35340 | A02 | 30383437 | C | T | missense_variant | MODERATE | c.328C>T|p.Pro110Ser |
S295 |
8 | BAA02g35340 | A02 | 30383709 | C | T | intron_variant | MODIFIER | c.374-22C>T| |
S149 |
9 | BAA02g35340 | A02 | 30385175 | C | T | missense_variant | MODERATE | c.1379C>T|p.Ala460Val |
S156 S275 |
10 | BAA02g35340 | A02 | 30386175 | C | T | missense_variant | MODERATE | c.2122C>T|p.Pro708Ser |
S108 |