Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g13150 | A03 | 5336415 | C | T | missense_variant | MODERATE | c.857G>A|p.Arg286Lys |
S293 |
2 | BAA03g13150 | A03 | 5336580 | G | A | missense_variant | MODERATE | c.773C>T|p.Thr258Ile |
S262 |
3 | BAA03g13150 | A03 | 5336688 | G | A | missense_variant | MODERATE | c.665C>T|p.Thr222Ile |
S135 |
4 | BAA03g13150 | A03 | 5336922 | C | T | missense_variant | MODERATE | c.505G>A|p.Glu169Lys |
S40 S49 |
5 | BAA03g13150 | A03 | 5337680 | G | A | missense_variant | MODERATE | c.121C>T|p.Leu41Phe |
S120 S157 S262 S263 |
6 | BAA03g13150 | A03 | 5338227 | G | A | upstream_gene_variant | MODIFIER | c.-130C>T| |
S68 |
7 | BAA03g13150 | A03 | 5341142 | G | A | upstream_gene_variant | MODIFIER | c.-3045C>T| |
S148 S30 S31 |
8 | BAA03g13150 | A03 | 5341186 | G | A | upstream_gene_variant | MODIFIER | c.-3089C>T| |
S245 |
9 | BAA03g13150 | A03 | 5341896 | C | T | upstream_gene_variant | MODIFIER | c.-3799G>A| |
S108 |