Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g23740 | A03 | 10892689 | G | A | upstream_gene_variant | MODIFIER | c.-3051G>A| |
S122 |
2 | BAA03g23740 | A03 | 10893150 | G | A | upstream_gene_variant | MODIFIER | c.-2590G>A| |
S139 |
3 | BAA03g23740 | A03 | 10893426 | G | A | upstream_gene_variant | MODIFIER | c.-2314G>A| |
S14 |
4 | BAA03g23740 | A03 | 10894258 | G | A | upstream_gene_variant | MODIFIER | c.-1482G>A| |
S294 |
5 | BAA03g23740 | A03 | 10895471 | A | T | upstream_gene_variant | MODIFIER | c.-269A>T| |
S169 |
6 | BAA03g23740 | A03 | 10896716 | C | T | missense_variant | MODERATE | c.359C>T|p.Ser120Phe |
S113 |
7 | BAA03g23740 | A03 | 10897276 | C | T | stop_gained | HIGH | c.721C>T|p.Gln241* |
S192 |
8 | BAA03g23740 | A03 | 10898463 | C | T | missense_variant | MODERATE | c.1351C>T|p.Pro451Ser |
S190 |
9 | BAA03g23740 | A03 | 10898467 | C | T | missense_variant | MODERATE | c.1355C>T|p.Ala452Val |
S158 |
10 | BAA03g23740 | A03 | 10898877 | C | T | missense_variant | MODERATE | c.1667C>T|p.Pro556Leu |
S164 |
11 | BAA03g23740 | A03 | 10899113 | C | T | missense_variant | MODERATE | c.1903C>T|p.His635Tyr |
S97 |