Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01000 | A04 | 589051 | C | T | missense_variant | MODERATE | c.364G>A|p.Val122Met |
S122 |
2 | BAA04g01000 | A04 | 589539 | G | A | synonymous_variant | LOW | c.210C>T|p.His70His |
S173 |
3 | BAA04g01000 | A04 | 590143 | G | A | upstream_gene_variant | MODIFIER | c.-395C>T| |
S156 |
4 | BAA04g01000 | A04 | 590619 | C | T | upstream_gene_variant | MODIFIER | c.-871G>A| |
S129 |
5 | BAA04g01000 | A04 | 593748 | G | A | upstream_gene_variant | MODIFIER | c.-4000C>T| |
S62 |
6 | BAA04g01000 | A04 | 593867 | C | T | upstream_gene_variant | MODIFIER | c.-4119G>A| |
S242 |
7 | BAA04g01000 | A04 | 594037 | G | A | upstream_gene_variant | MODIFIER | c.-4289C>T| |
S245 |
8 | BAA04g01000 | A04 | 594581 | G | A | upstream_gene_variant | MODIFIER | c.-4833C>T| |
S166 |