Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g39940 | A05 | 38848243 | G | A | missense_variant | MODERATE | c.55G>A|p.Glu19Lys |
S98 |
2 | BAA05g39940 | A05 | 38849174 | G | A | missense_variant | MODERATE | c.818G>A|p.Cys273Tyr |
S132 S137 S240 |
3 | BAA05g39940 | A05 | 38849299 | G | A | missense_variant | MODERATE | c.943G>A|p.Glu315Lys |
S74 |
4 | BAA05g39940 | A05 | 38849501 | C | T | missense_variant | MODERATE | c.1145C>T|p.Ala382Val |
S36 |
5 | BAA05g39940 | A05 | 38849534 | C | T | missense_variant | MODERATE | c.1178C>T|p.Pro393Leu |
S47 |
6 | BAA05g39940 | A05 | 38849650 | G | A | missense_variant | MODERATE | c.1294G>A|p.Ala432Thr |
S281 |
7 | BAA05g39940 | A05 | 38849862 | C | T | synonymous_variant | LOW | c.1506C>T|p.Ser502Ser |
S115 |
8 | BAA05g39940 | A05 | 38849900 | C | T | missense_variant | MODERATE | c.1544C>T|p.Ser515Leu |
S65 |
9 | BAA05g39940 | A05 | 38850459 | G | A | synonymous_variant | LOW | c.2103G>A|p.Val701Val |
S143 |
10 | BAA05g39940 | A05 | 38850555 | G | A | synonymous_variant | LOW | c.2199G>A|p.Pro733Pro |
S74 |
11 | BAA05g39940 | A05 | 38852512 | G | A | downstream_gene_variant | MODIFIER | c.*1813G>A| |
S200 S46 |