Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00180 | A08 | 158186 | C | A | upstream_gene_variant | MODIFIER | c.-4697C>A| |
S103 |
2 | BAA08g00180 | A08 | 159758 | C | T | upstream_gene_variant | MODIFIER | c.-3125C>T| |
S156 |
3 | BAA08g00180 | A08 | 161230 | G | A | upstream_gene_variant | MODIFIER | c.-1653G>A| |
S13 |
4 | BAA08g00180 | A08 | 162547 | C | T | upstream_gene_variant | MODIFIER | c.-336C>T| |
S206 S26 |
5 | BAA08g00180 | A08 | 162686 | G | A | upstream_gene_variant | MODIFIER | c.-197G>A| |
S262 |
6 | BAA08g00180 | A08 | 163350 | G | A | intron_variant | MODIFIER | c.202+266G>A| |
S8 S90 |
7 | BAA08g00180 | A08 | 167013 | G | A | missense_variant | MODERATE | c.730G>A|p.Glu244Lys |
S260 |
8 | BAA08g00180 | A08 | 167021 | G | A | synonymous_variant | LOW | c.738G>A|p.Glu246Glu |
S64 |
9 | BAA08g00180 | A08 | 168073 | C | T | downstream_gene_variant | MODIFIER | c.*824C>T| |
S136 |
10 | BAA08g00180 | A08 | 168225 | G | A | downstream_gene_variant | MODIFIER | c.*976G>A| |
S33 |