Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02600 | A02 | 1173836 | C | T | upstream_gene_variant | MODIFIER | c.-874C>T| |
S152 |
2 | BAA02g02600 | A02 | 1173858 | G | A | upstream_gene_variant | MODIFIER | c.-852G>A| |
S105 S106 |
3 | BAA02g02600 | A02 | 1173969 | G | A | upstream_gene_variant | MODIFIER | c.-741G>A| |
S231 |
4 | BAA02g02600 | A02 | 1174041 | G | A | upstream_gene_variant | MODIFIER | c.-669G>A| |
S23 |
5 | BAA02g02600 | A02 | 1174582 | C | T | upstream_gene_variant | MODIFIER | c.-128C>T| |
S39 |
6 | BAA02g02600 | A02 | 1174583 | G | A | upstream_gene_variant | MODIFIER | c.-127G>A| |
S68 |
7 | BAA02g02600 | A02 | 1174934 | G | A | splice_region_variant&intron_variant | LOW | c.135+8G>A| |
S52 |
8 | BAA02g02600 | A02 | 1176675 | G | A | missense_variant | MODERATE | c.587G>A|p.Gly196Asp |
S41 |
9 | BAA02g02600 | A02 | 1182599 | G | A | downstream_gene_variant | MODIFIER | c.*4341G>A| |
S23 |