Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g26600 | A08 | 18968967 | C | T | upstream_gene_variant | MODIFIER | c.-1678C>T| |
S299 |
2 | BAA08g26600 | A08 | 18969340 | G | A | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S36 |
3 | BAA08g26600 | A08 | 18969407 | C | T | upstream_gene_variant | MODIFIER | c.-1238C>T| |
S19 |
4 | BAA08g26600 | A08 | 18969477 | A | T | upstream_gene_variant | MODIFIER | c.-1168A>T| |
S9 |
5 | BAA08g26600 | A08 | 18969669 | C | T | upstream_gene_variant | MODIFIER | c.-976C>T| |
S208 S219 |
6 | BAA08g26600 | A08 | 18970514 | C | T | upstream_gene_variant | MODIFIER | c.-131C>T| |
S148 S210 S30 S31 |
7 | BAA08g26600 | A08 | 18970767 | C | T | synonymous_variant | LOW | c.123C>T|p.Leu41Leu |
S252 |
8 | BAA08g26600 | A08 | 18971380 | C | T | synonymous_variant | LOW | c.528C>T|p.Phe176Phe |
S236 |
9 | BAA08g26600 | A08 | 18971459 | C | T | synonymous_variant | LOW | c.607C>T|p.Leu203Leu |
S152 |
10 | BAA08g26600 | A08 | 18971714 | C | T | missense_variant | MODERATE | c.767C>T|p.Ala256Val |
S210 |
11 | BAA08g26600 | A08 | 18971737 | C | T | synonymous_variant | LOW | c.790C>T|p.Leu264Leu |
S53 |