Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g42060 | A09 | 48595232 | G | A | upstream_gene_variant | MODIFIER | c.-4190G>A| |
S143 |
2 | BAA09g42060 | A09 | 48595571 | G | A | upstream_gene_variant | MODIFIER | c.-3851G>A| |
S59 |
3 | BAA09g42060 | A09 | 48595637 | G | A | upstream_gene_variant | MODIFIER | c.-3785G>A| |
S221 |
4 | BAA09g42060 | A09 | 48596546 | G | A | upstream_gene_variant | MODIFIER | c.-2876G>A| |
S181 |
5 | BAA09g42060 | A09 | 48597225 | G | A | upstream_gene_variant | MODIFIER | c.-2197G>A| |
S158 |
6 | BAA09g42060 | A09 | 48597623 | C | T | upstream_gene_variant | MODIFIER | c.-1799C>T| |
S216 S241 S39 |
7 | BAA09g42060 | A09 | 48598261 | G | A | upstream_gene_variant | MODIFIER | c.-1161G>A| |
S25 |
8 | BAA09g42060 | A09 | 48598489 | C | T | upstream_gene_variant | MODIFIER | c.-933C>T| |
S124 |
9 | BAA09g42060 | A09 | 48599338 | G | A | upstream_gene_variant | MODIFIER | c.-84G>A| |
S126 |
10 | BAA09g42060 | A09 | 48599593 | C | T | missense_variant | MODERATE | c.172C>T|p.Arg58Cys |
S19 |
11 | BAA09g42060 | A09 | 48599620 | C | T | missense_variant | MODERATE | c.199C>T|p.Pro67Ser |
S37 |
12 | BAA09g42060 | A09 | 48601332 | C | T | missense_variant | MODERATE | c.773C>T|p.Pro258Leu |
S95 |