Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10400 | A02 | 4601541 | C | T | missense_variant | MODERATE | c.593G>A|p.Ser198Asn |
S185 |
2 | BAA02g10400 | A02 | 4601545 | C | T | missense_variant | MODERATE | c.589G>A|p.Gly197Arg |
S139 |
3 | BAA02g10400 | A02 | 4605575 | G | A | upstream_gene_variant | MODIFIER | c.-2718C>T| |
S156 |
4 | BAA02g10400 | A02 | 4605840 | G | A | upstream_gene_variant | MODIFIER | c.-2983C>T| |
S20 |
5 | BAA02g10400 | A02 | 4607048 | C | T | upstream_gene_variant | MODIFIER | c.-4191G>A| |
S38 |
6 | BAA02g10400 | A02 | 4607179 | C | T | upstream_gene_variant | MODIFIER | c.-4322G>A| |
S292 |
7 | BAA02g10400 | A02 | 4607400 | C | T | upstream_gene_variant | MODIFIER | c.-4543G>A| |
S103 |
8 | BAA02g10400 | A02 | 4607516 | C | T | upstream_gene_variant | MODIFIER | c.-4659G>A| |
S73 S91 |