Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g45470 | A03 | 21769614 | C | T | upstream_gene_variant | MODIFIER | c.-116C>T| |
S216 |
2 | BAA03g45470 | A03 | 21769946 | C | T | intron_variant | MODIFIER | c.135+82C>T| |
S255 |
3 | BAA03g45470 | A03 | 21770560 | C | T | synonymous_variant | LOW | c.340C>T|p.Leu114Leu |
S206 S26 |
4 | BAA03g45470 | A03 | 21771197 | G | A | stop_gained | HIGH | c.516G>A|p.Trp172* |
S292 |
5 | BAA03g45470 | A03 | 21771542 | C | T | missense_variant | MODERATE | c.667C>T|p.Pro223Ser |
S264 |
6 | BAA03g45470 | A03 | 21772488 | C | T | missense_variant | MODERATE | c.1067C>T|p.Ser356Leu |
S53 |
7 | BAA03g45470 | A03 | 21773325 | C | T | synonymous_variant | LOW | c.1621C>T|p.Leu541Leu |
S295 |
8 | BAA03g45470 | A03 | 21773718 | C | T | synonymous_variant | LOW | c.1929C>T|p.Phe643Phe |
S241 |
9 | BAA03g45470 | A03 | 21774387 | C | T | splice_region_variant&intron_variant | LOW | c.2170-7C>T| |
S242 |
10 | BAA03g45470 | A03 | 21774598 | G | A | missense_variant | MODERATE | c.2374G>A|p.Glu792Lys |
S142 |
11 | BAA03g45470 | A03 | 21774647 | G | A | missense_variant | MODERATE | c.2423G>A|p.Arg808Lys |
S286 |
12 | BAA03g45470 | A03 | 21774980 | C | T | missense_variant | MODERATE | c.2756C>T|p.Ser919Phe |
S165 |