Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11670 | A01 | 5404845 | C | T | missense_variant | MODERATE | c.76C>T|p.Pro26Ser |
S20 |
2 | BAA01g11670 | A01 | 5405277 | G | A | missense_variant | MODERATE | c.293G>A|p.Gly98Asp |
S293 |
3 | BAA01g11670 | A01 | 5405648 | C | T | missense_variant | MODERATE | c.664C>T|p.Pro222Ser |
S64 |
4 | BAA01g11670 | A01 | 5405897 | G | A | missense_variant | MODERATE | c.791G>A|p.Gly264Glu |
S218 |
5 | BAA01g11670 | A01 | 5405991 | C | T | synonymous_variant | LOW | c.885C>T|p.Pro295Pro |
S231 |
6 | BAA01g11670 | A01 | 5409660 | C | T | downstream_gene_variant | MODIFIER | c.*3633C>T| |
S136 |
7 | BAA01g11670 | A01 | 5410392 | C | T | downstream_gene_variant | MODIFIER | c.*4365C>T| |
S185 |