Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g05920 | A05 | 2847564 | C | T | stop_gained | HIGH | c.2265G>A|p.Trp755* |
S135 |
2 | BAA05g05920 | A05 | 2848602 | G | A | synonymous_variant | LOW | c.1602C>T|p.Tyr534Tyr |
S299 |
3 | BAA05g05920 | A05 | 2848717 | C | T | missense_variant | MODERATE | c.1487G>A|p.Arg496Lys |
S89 |
4 | BAA05g05920 | A05 | 2849438 | C | T | missense_variant | MODERATE | c.766G>A|p.Val256Ile |
S108 |
5 | BAA05g05920 | A05 | 2849462 | C | T | missense_variant | MODERATE | c.742G>A|p.Val248Ile |
S62 |
6 | BAA05g05920 | A05 | 2849655 | C | T | synonymous_variant | LOW | c.549G>A|p.Ala183Ala |
S53 |
7 | BAA05g05920 | A05 | 2850132 | C | T | missense_variant | MODERATE | c.337G>A|p.Ala113Thr |
S164 |
8 | BAA05g05920 | A05 | 2850614 | G | A | missense_variant | MODERATE | c.5C>T|p.Ala2Val |
S221 |
9 | BAA05g05920 | A05 | 2850766 | C | T | upstream_gene_variant | MODIFIER | c.-148G>A| |
S71 |
10 | BAA05g05920 | A05 | 2851883 | G | A | upstream_gene_variant | MODIFIER | c.-1265C>T| |
S111 |
11 | BAA05g05920 | A05 | 2851995 | C | T | upstream_gene_variant | MODIFIER | c.-1377G>A| |
S203 |
12 | BAA05g05920 | A05 | 2853562 | C | T | upstream_gene_variant | MODIFIER | c.-2944G>A| |
S162 |
13 | BAA05g05920 | A05 | 2853827 | G | A | upstream_gene_variant | MODIFIER | c.-3209C>T| |
S167 S236 S257 S262 |
14 | BAA05g05920 | A05 | 2854156 | C | T | upstream_gene_variant | MODIFIER | c.-3538G>A| |
S9 |