Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11460 | A08 | 10158146 | C | T | downstream_gene_variant | MODIFIER | c.*4143G>A| |
S219 |
2 | BAA08g11460 | A08 | 10162540 | G | A | missense_variant | MODERATE | c.166C>T|p.Pro56Ser |
S289 S290 |
3 | BAA08g11460 | A08 | 10164296 | G | A | upstream_gene_variant | MODIFIER | c.-1591C>T| |
S246 |
4 | BAA08g11460 | A08 | 10165350 | G | A | upstream_gene_variant | MODIFIER | c.-2645C>T| |
S301 S304 |
5 | BAA08g11460 | A08 | 10166300 | G | A | upstream_gene_variant | MODIFIER | c.-3595C>T| |
S286 |
6 | BAA08g11460 | A08 | 10166327 | G | A | upstream_gene_variant | MODIFIER | c.-3622C>T| |
S286 |
7 | BAA08g11460 | A08 | 10166736 | T | C | upstream_gene_variant | MODIFIER | c.-4031A>G| |
S245 |
8 | BAA08g11460 | A08 | 10166938 | G | A | upstream_gene_variant | MODIFIER | c.-4233C>T| |
S158 |
9 | BAA08g11460 | A08 | 10166969 | C | T | upstream_gene_variant | MODIFIER | c.-4264G>A| |
S250 |
10 | BAA08g11460 | A08 | 10167633 | G | A | upstream_gene_variant | MODIFIER | c.-4928C>T| |
S61 |