Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g03360 | A09 | 2045193 | C | T | missense_variant | MODERATE | c.61G>A|p.Asp21Asn |
S9 |
2 | BAA09g03360 | A09 | 2045416 | G | A | upstream_gene_variant | MODIFIER | c.-163C>T| |
S81 S85 |
3 | BAA09g03360 | A09 | 2045645 | G | A | upstream_gene_variant | MODIFIER | c.-392C>T| |
S294 |
4 | BAA09g03360 | A09 | 2045723 | C | T | upstream_gene_variant | MODIFIER | c.-470G>A| |
S86 |
5 | BAA09g03360 | A09 | 2046487 | C | T | upstream_gene_variant | MODIFIER | c.-1234G>A| |
S151 |
6 | BAA09g03360 | A09 | 2047961 | G | A | upstream_gene_variant | MODIFIER | c.-2708C>T| |
S127 |
7 | BAA09g03360 | A09 | 2047984 | G | A | upstream_gene_variant | MODIFIER | c.-2731C>T| |
S223 |
8 | BAA09g03360 | A09 | 2049667 | C | T | upstream_gene_variant | MODIFIER | c.-4414G>A| |
S58 |
9 | BAA09g03360 | A09 | 2049774 | G | A | upstream_gene_variant | MODIFIER | c.-4521C>T| |
S4 |