Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05830 | A01 | 2600629 | C | T | missense_variant | MODERATE | c.3962G>A|p.Arg1321Gln |
S40 S49 |
2 | BAA01g05830 | A01 | 2601805 | C | T | missense_variant | MODERATE | c.3037G>A|p.Glu1013Lys |
S77 S82 |
3 | BAA01g05830 | A01 | 2601828 | G | A | missense_variant | MODERATE | c.3014C>T|p.Ser1005Phe |
S165 |
4 | BAA01g05830 | A01 | 2602420 | C | T | missense_variant | MODERATE | c.2422G>A|p.Val808Met |
S157 S166 S167 S262 |
5 | BAA01g05830 | A01 | 2604659 | C | T | synonymous_variant | LOW | c.270G>A|p.Glu90Glu |
S104 S52 |
6 | BAA01g05830 | A01 | 2605909 | C | T | upstream_gene_variant | MODIFIER | c.-981G>A| |
S140 |
7 | BAA01g05830 | A01 | 2606055 | G | A | upstream_gene_variant | MODIFIER | c.-1127C>T| |
S197 |
8 | BAA01g05830 | A01 | 2607139 | G | A | upstream_gene_variant | MODIFIER | c.-2211C>T| |
S274 |
9 | BAA01g05830 | A01 | 2607948 | G | A | upstream_gene_variant | MODIFIER | c.-3020C>T| |
S197 |
10 | BAA01g05830 | A01 | 2607957 | C | T | upstream_gene_variant | MODIFIER | c.-3029G>A| |
S41 |
11 | BAA01g05830 | A01 | 2608594 | C | A | upstream_gene_variant | MODIFIER | c.-3666G>T| |
S159 S182 S240 S274 S275 S283 S284 S289 S298 S304 S42 S43 S58 |
12 | BAA01g05830 | A01 | 2608752 | G | A | upstream_gene_variant | MODIFIER | c.-3824C>T| |
S242 |