Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17600 | A02 | 8774171 | C | T | missense_variant | MODERATE | c.143C>T|p.Pro48Leu |
S273 |
2 | BAA02g17600 | A02 | 8774377 | G | A | missense_variant | MODERATE | c.349G>A|p.Val117Ile |
S223 |
3 | BAA02g17600 | A02 | 8774681 | C | T | missense_variant | MODERATE | c.524C>T|p.Ser175Phe |
S84 S93 |
4 | BAA02g17600 | A02 | 8774835 | C | T | missense_variant | MODERATE | c.584C>T|p.Ala195Val |
S255 |
5 | BAA02g17600 | A02 | 8775186 | C | T | synonymous_variant | LOW | c.700C>T|p.Leu234Leu |
S234 |
6 | BAA02g17600 | A02 | 8775628 | G | A | missense_variant | MODERATE | c.823G>A|p.Val275Ile |
S205 |
7 | BAA02g17600 | A02 | 8777124 | C | T | synonymous_variant | LOW | c.1540C>T|p.Leu514Leu |
S201 |
8 | BAA02g17600 | A02 | 8777176 | G | A | missense_variant | MODERATE | c.1592G>A|p.Ser531Asn |
S50 |
9 | BAA02g17600 | A02 | 8777447 | C | T | downstream_gene_variant | MODIFIER | c.*252C>T| |
S163 |
10 | BAA02g17600 | A02 | 8778384 | C | T | downstream_gene_variant | MODIFIER | c.*1189C>T| |
S9 |
11 | BAA02g17600 | A02 | 8778760 | G | A | downstream_gene_variant | MODIFIER | c.*1565G>A| |
S155 S211 |