Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21390 | A02 | 11469642 | C | T | upstream_gene_variant | MODIFIER | c.-4730C>T| |
S177 |
2 | BAA02g21390 | A02 | 11472056 | G | A | upstream_gene_variant | MODIFIER | c.-2316G>A| |
S168 |
3 | BAA02g21390 | A02 | 11472078 | G | A | upstream_gene_variant | MODIFIER | c.-2294G>A| |
S168 |
4 | BAA02g21390 | A02 | 11474471 | C | T | missense_variant | MODERATE | c.100C>T|p.His34Tyr |
S138 |
5 | BAA02g21390 | A02 | 11475004 | C | T | synonymous_variant | LOW | c.474C>T|p.Ser158Ser |
S51 |
6 | BAA02g21390 | A02 | 11480149 | C | T | intron_variant | MODIFIER | c.584-228C>T| |
S87 |
7 | BAA02g21390 | A02 | 11485312 | T | G | downstream_gene_variant | MODIFIER | c.*4412T>G| |
S191 |
8 | BAA02g21390 | A02 | 11485432 | G | A | downstream_gene_variant | MODIFIER | c.*4532G>A| |
S231 |
9 | BAA02g21390 | A02 | 11485485 | C | T | downstream_gene_variant | MODIFIER | c.*4585C>T| |
S289 |