Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g12000 | A07 | 20486754 | G | A | missense_variant | MODERATE | c.1405C>T|p.Leu469Phe |
S73 S91 |
2 | BAA07g12000 | A07 | 20487653 | C | T | missense_variant | MODERATE | c.506G>A|p.Arg169Lys |
S97 |
3 | BAA07g12000 | A07 | 20487694 | G | A | synonymous_variant | LOW | c.465C>T|p.Phe155Phe |
S236 |
4 | BAA07g12000 | A07 | 20487908 | C | T | missense_variant | MODERATE | c.251G>A|p.Arg84His |
S32 |
5 | BAA07g12000 | A07 | 20488244 | G | T | upstream_gene_variant | MODIFIER | c.-86C>A| |
S122 S153 S156 S159 S181 S190 S213 S227 S26 S301 S69 S7 S74 |
6 | BAA07g12000 | A07 | 20488921 | G | A | upstream_gene_variant | MODIFIER | c.-763C>T| |
S134 |
7 | BAA07g12000 | A07 | 20489002 | C | T | upstream_gene_variant | MODIFIER | c.-844G>A| |
S120 |
8 | BAA07g12000 | A07 | 20489085 | G | A | upstream_gene_variant | MODIFIER | c.-927C>T| |
S292 S98 |
9 | BAA07g12000 | A07 | 20490868 | G | A | upstream_gene_variant | MODIFIER | c.-2710C>T| |
S65 |
10 | BAA07g12000 | A07 | 20491283 | G | A | upstream_gene_variant | MODIFIER | c.-3125C>T| |
S190 |
11 | BAA07g12000 | A07 | 20491484 | C | T | upstream_gene_variant | MODIFIER | c.-3326G>A| |
S4 |
12 | BAA07g12000 | A07 | 20492740 | G | A | upstream_gene_variant | MODIFIER | c.-4582C>T| |
S61 |