Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19390 | A09 | 11805473 | G | A | intron_variant | MODIFIER | c.141-42C>T| |
S66 |
2 | BAA09g19390 | A09 | 11806083 | T | C | upstream_gene_variant | MODIFIER | c.-338A>G| |
S301 S304 |
3 | BAA09g19390 | A09 | 11806143 | G | A | upstream_gene_variant | MODIFIER | c.-398C>T| |
S40 S49 |
4 | BAA09g19390 | A09 | 11806376 | G | A | upstream_gene_variant | MODIFIER | c.-631C>T| |
S79 S91 |
5 | BAA09g19390 | A09 | 11806568 | G | A | upstream_gene_variant | MODIFIER | c.-823C>T| |
S210 |
6 | BAA09g19390 | A09 | 11807169 | G | A | upstream_gene_variant | MODIFIER | c.-1424C>T| |
S144 |
7 | BAA09g19390 | A09 | 11807369 | G | A | upstream_gene_variant | MODIFIER | c.-1624C>T| |
S251 |
8 | BAA09g19390 | A09 | 11809589 | G | A | upstream_gene_variant | MODIFIER | c.-3844C>T| |
S251 |
9 | BAA09g19390 | A09 | 11809917 | C | A | upstream_gene_variant | MODIFIER | c.-4172G>T| |
S53 |