Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44200 | A02 | 36485969 | C | T | downstream_gene_variant | MODIFIER | c.*3445G>A| |
S58 |
2 | BAA02g44200 | A02 | 36490943 | G | A | missense_variant | MODERATE | c.217C>T|p.Pro73Ser |
S291 |
3 | BAA02g44200 | A02 | 36491035 | C | T | missense_variant | MODERATE | c.125G>A|p.Gly42Glu |
S87 |
4 | BAA02g44200 | A02 | 36491051 | G | A | missense_variant | MODERATE | c.109C>T|p.Arg37Trp |
S264 |
5 | BAA02g44200 | A02 | 36491092 | C | T | missense_variant | MODERATE | c.68G>A|p.Arg23His |
S48 |
6 | BAA02g44200 | A02 | 36491386 | G | A | upstream_gene_variant | MODIFIER | c.-227C>T| |
S20 |
7 | BAA02g44200 | A02 | 36491960 | C | T | upstream_gene_variant | MODIFIER | c.-801G>A| |
S256 |
8 | BAA02g44200 | A02 | 36493704 | G | A | upstream_gene_variant | MODIFIER | c.-2545C>T| |
S139 |
9 | BAA02g44200 | A02 | 36494898 | G | A | upstream_gene_variant | MODIFIER | c.-3739C>T| |
S103 |
10 | BAA02g44200 | A02 | 36495384 | G | A | upstream_gene_variant | MODIFIER | c.-4225C>T| |
S213 |