Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g05690 | A09 | 3237111 | C | T | missense_variant | MODERATE | c.1462G>A|p.Glu488Lys |
S77 S82 |
2 | BAA09g05690 | A09 | 3237996 | C | T | missense_variant | MODERATE | c.1119G>A|p.Met373Ile |
S71 |
3 | BAA09g05690 | A09 | 3238303 | C | T | missense_variant | MODERATE | c.970G>A|p.Glu324Lys |
S287 |
4 | BAA09g05690 | A09 | 3238695 | G | A | missense_variant | MODERATE | c.748C>T|p.Leu250Phe |
S231 |
5 | BAA09g05690 | A09 | 3240042 | G | A | missense_variant | MODERATE | c.68C>T|p.Ser23Phe |
S142 |
6 | BAA09g05690 | A09 | 3240075 | C | T | missense_variant | MODERATE | c.35G>A|p.Arg12His |
S303 |
7 | BAA09g05690 | A09 | 3240870 | G | A | upstream_gene_variant | MODIFIER | c.-761C>T| |
S306 S308 |
8 | BAA09g05690 | A09 | 3241285 | G | A | upstream_gene_variant | MODIFIER | c.-1176C>T| |
S201 |
9 | BAA09g05690 | A09 | 3241311 | C | T | upstream_gene_variant | MODIFIER | c.-1202G>A| |
S46 |
10 | BAA09g05690 | A09 | 3241451 | G | A | upstream_gene_variant | MODIFIER | c.-1342C>T| |
S20 |
11 | BAA09g05690 | A09 | 3242647 | C | T | upstream_gene_variant | MODIFIER | c.-2538G>A| |
S132 S137 S215 |
12 | BAA09g05690 | A09 | 3243803 | G | A | upstream_gene_variant | MODIFIER | c.-3694C>T| |
S125 |