Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28820 | A01 | 18104302 | C | T | upstream_gene_variant | MODIFIER | c.-4781C>T| |
S200 |
2 | BAA01g28820 | A01 | 18110641 | C | T | missense_variant | MODERATE | c.662C>T|p.Ser221Phe |
S204 |
3 | BAA01g28820 | A01 | 18110722 | C | T | missense_variant | MODERATE | c.743C>T|p.Thr248Met |
S167 |
4 | BAA01g28820 | A01 | 18112998 | G | A | intron_variant | MODIFIER | c.970+810G>A| |
S207 |
5 | BAA01g28820 | A01 | 18113318 | G | A | intron_variant | MODIFIER | c.970+1130G>A| |
S124 |
6 | BAA01g28820 | A01 | 18113770 | G | A | intron_variant | MODIFIER | c.970+1582G>A| |
S9 |
7 | BAA01g28820 | A01 | 18115539 | C | T | intron_variant | MODIFIER | c.970+3351C>T| |
S205 |
8 | BAA01g28820 | A01 | 18115970 | G | A | intron_variant | MODIFIER | c.970+3782G>A| |
S308 |
9 | BAA01g28820 | A01 | 18117119 | G | A | intron_variant | MODIFIER | c.970+4931G>A| |
S12 |
10 | BAA01g28820 | A01 | 18117461 | A | C | intron_variant | MODIFIER | c.971-4769A>C| |
S58 |
11 | BAA01g28820 | A01 | 18121371 | G | A | intron_variant | MODIFIER | c.971-859G>A| |
S103 |
12 | BAA01g28820 | A01 | 18121502 | C | T | intron_variant | MODIFIER | c.971-728C>T| |
S240 |
13 | BAA01g28820 | A01 | 18123888 | G | A | downstream_gene_variant | MODIFIER | c.*866G>A| |
S1 S90 |
14 | BAA01g28820 | A01 | 18124612 | C | T | downstream_gene_variant | MODIFIER | c.*1590C>T| |
S117 |
15 | BAA01g28820 | A01 | 18125517 | G | A | downstream_gene_variant | MODIFIER | c.*2495G>A| |
S124 |
16 | BAA01g28820 | A01 | 18126581 | G | A | downstream_gene_variant | MODIFIER | c.*3559G>A| |
S61 |