Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g20440 | A05 | 12589953 | A | T | upstream_gene_variant | MODIFIER | c.-2148A>T| |
S2 |
2 | BAA05g20440 | A05 | 12591846 | G | A | upstream_gene_variant | MODIFIER | c.-255G>A| |
S112 |
3 | BAA05g20440 | A05 | 12592562 | A | G | synonymous_variant | LOW | c.462A>G|p.Ser154Ser |
S129 |
4 | BAA05g20440 | A05 | 12592735 | G | A | intron_variant | MODIFIER | c.573+62G>A| |
S212 |
5 | BAA05g20440 | A05 | 12592874 | G | A | stop_gained | HIGH | c.603G>A|p.Trp201* |
S284 |
6 | BAA05g20440 | A05 | 12593499 | C | T | missense_variant | MODERATE | c.1228C>T|p.Pro410Ser |
S2 |
7 | BAA05g20440 | A05 | 12593521 | G | A | missense_variant | MODERATE | c.1250G>A|p.Gly417Glu |
S197 |
8 | BAA05g20440 | A05 | 12593582 | G | A | stop_gained | HIGH | c.1311G>A|p.Trp437* |
S122 |
9 | BAA05g20440 | A05 | 12598958 | C | T | downstream_gene_variant | MODIFIER | c.*3012C>T| |
S153 S213 |
10 | BAA05g20440 | A05 | 12599187 | C | T | downstream_gene_variant | MODIFIER | c.*3241C>T| |
S247 |
11 | BAA05g20440 | A05 | 12599727 | C | T | downstream_gene_variant | MODIFIER | c.*3781C>T| |
S36 |
12 | BAA05g20440 | A05 | 12600204 | G | A | downstream_gene_variant | MODIFIER | c.*4258G>A| |
S266 |
13 | BAA05g20440 | A05 | 12600890 | G | A | downstream_gene_variant | MODIFIER | c.*4944G>A| |
S276 |