Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16960 | A02 | 8404867 | C | T | missense_variant | MODERATE | c.1538G>A|p.Gly513Glu |
S55 |
2 | BAA02g16960 | A02 | 8405272 | C | T | missense_variant | MODERATE | c.1315G>A|p.Ala439Thr |
S123 |
3 | BAA02g16960 | A02 | 8406533 | C | T | missense_variant | MODERATE | c.301G>A|p.Asp101Asn |
S131 |
4 | BAA02g16960 | A02 | 8406562 | C | T | missense_variant | MODERATE | c.272G>A|p.Gly91Glu |
S71 |
5 | BAA02g16960 | A02 | 8407401 | C | T | upstream_gene_variant | MODIFIER | c.-54G>A| |
S108 |
6 | BAA02g16960 | A02 | 8408420 | G | A | upstream_gene_variant | MODIFIER | c.-1073C>T| |
S11 |
7 | BAA02g16960 | A02 | 8410214 | C | T | upstream_gene_variant | MODIFIER | c.-2867G>A| |
S178 |
8 | BAA02g16960 | A02 | 8410418 | G | A | upstream_gene_variant | MODIFIER | c.-3071C>T| |
S19 |