Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g08640 | A01 | 3818343 | G | A | missense_variant | MODERATE | c.434G>A|p.Gly145Glu |
S95 |
2 | BAA01g08640 | A01 | 3818493 | C | T | missense_variant | MODERATE | c.584C>T|p.Pro195Leu |
S2 |
3 | BAA01g08640 | A01 | 3818497 | G | A | missense_variant | MODERATE | c.588G>A|p.Met196Ile |
S95 |
4 | BAA01g08640 | A01 | 3818568 | G | A | missense_variant | MODERATE | c.659G>A|p.Gly220Glu |
S292 |
5 | BAA01g08640 | A01 | 3818574 | G | A | missense_variant | MODERATE | c.665G>A|p.Gly222Glu |
S10 |
6 | BAA01g08640 | A01 | 3818613 | C | T | missense_variant | MODERATE | c.704C>T|p.Ser235Phe |
S244 |
7 | BAA01g08640 | A01 | 3818684 | G | A | missense_variant | MODERATE | c.775G>A|p.Ala259Thr |
S272 |
8 | BAA01g08640 | A01 | 3818758 | T | C | synonymous_variant | LOW | c.849T>C|p.Leu283Leu |
S42 |
9 | BAA01g08640 | A01 | 3818837 | G | A | missense_variant | MODERATE | c.928G>A|p.Glu310Lys |
S216 |
10 | BAA01g08640 | A01 | 3818865 | C | T | missense_variant | MODERATE | c.956C>T|p.Ala319Val |
S250 |
11 | BAA01g08640 | A01 | 3819317 | G | A | missense_variant | MODERATE | c.1333G>A|p.Asp445Asn |
S281 |
12 | BAA01g08640 | A01 | 3824212 | C | T | downstream_gene_variant | MODIFIER | c.*4407C>T| |
S185 |