Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28480 | A02 | 16011701 | G | A | missense_variant | MODERATE | c.1216C>T|p.Pro406Ser |
S57 |
2 | BAA02g28480 | A02 | 16012166 | G | T | synonymous_variant | LOW | c.939C>A|p.Leu313Leu |
S70 |
3 | BAA02g28480 | A02 | 16012879 | G | A | synonymous_variant | LOW | c.372C>T|p.Asn124Asn |
S209 |
4 | BAA02g28480 | A02 | 16012972 | G | A | synonymous_variant | LOW | c.279C>T|p.His93His |
S251 |
5 | BAA02g28480 | A02 | 16013208 | G | A | missense_variant | MODERATE | c.43C>T|p.Leu15Phe |
S97 |
6 | BAA02g28480 | A02 | 16014812 | G | A | upstream_gene_variant | MODIFIER | c.-1562C>T| |
S297 |
7 | BAA02g28480 | A02 | 16017819 | G | A | upstream_gene_variant | MODIFIER | c.-4569C>T| |
S130 |
8 | BAA02g28480 | A02 | 16017910 | G | A | upstream_gene_variant | MODIFIER | c.-4660C>T| |
S161 |
9 | BAA02g28480 | A02 | 16018006 | C | T | upstream_gene_variant | MODIFIER | c.-4756G>A| |
S177 |