Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10560 | A01 | 4844125 | G | A | missense_variant | MODERATE | c.53G>A|p.Gly18Asp |
S11 |
2 | BAA01g10560 | A01 | 4845581 | G | A | missense_variant | MODERATE | c.982G>A|p.Ala328Thr |
S279 |
3 | BAA01g10560 | A01 | 4845650 | G | A | missense_variant | MODERATE | c.1051G>A|p.Glu351Lys |
S123 |
4 | BAA01g10560 | A01 | 4846398 | C | T | synonymous_variant | LOW | c.1647C>T|p.Asn549Asn |
S221 |
5 | BAA01g10560 | A01 | 4846528 | C | T | stop_gained | HIGH | c.1777C>T|p.Gln593* |
S136 |
6 | BAA01g10560 | A01 | 4846628 | C | T | missense_variant | MODERATE | c.1877C>T|p.Ala626Val |
S112 |
7 | BAA01g10560 | A01 | 4852374 | C | T | downstream_gene_variant | MODIFIER | c.*4893C>T| |
S76 |