Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g07780 | A09 | 4310412 | C | T | upstream_gene_variant | MODIFIER | c.-4539C>T| |
S54 |
2 | BAA09g07780 | A09 | 4312165 | G | A | upstream_gene_variant | MODIFIER | c.-2786G>A| |
S45 |
3 | BAA09g07780 | A09 | 4312261 | C | T | upstream_gene_variant | MODIFIER | c.-2690C>T| |
S135 |
4 | BAA09g07780 | A09 | 4313278 | G | A | upstream_gene_variant | MODIFIER | c.-1673G>A| |
S219 |
5 | BAA09g07780 | A09 | 4314985 | C | T | missense_variant | MODERATE | c.35C>T|p.Ser12Phe |
S284 |
6 | BAA09g07780 | A09 | 4314996 | G | A | missense_variant | MODERATE | c.46G>A|p.Glu16Lys |
S44 |
7 | BAA09g07780 | A09 | 4315722 | G | A | missense_variant | MODERATE | c.587G>A|p.Gly196Asp |
S218 |
8 | BAA09g07780 | A09 | 4316349 | G | A | missense_variant | MODERATE | c.1051G>A|p.Gly351Arg |
S219 |
9 | BAA09g07780 | A09 | 4317196 | C | T | missense_variant | MODERATE | c.1582C>T|p.Pro528Ser |
S302 |
10 | BAA09g07780 | A09 | 4322077 | G | A | downstream_gene_variant | MODIFIER | c.*4837G>A| |
S122 S74 |