Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11020 | A02 | 4968274 | G | A | upstream_gene_variant | MODIFIER | c.-2746G>A| |
S168 |
2 | BAA02g11020 | A02 | 4969331 | C | T | upstream_gene_variant | MODIFIER | c.-1689C>T| |
S42 |
3 | BAA02g11020 | A02 | 4969967 | C | T | upstream_gene_variant | MODIFIER | c.-1053C>T| |
S264 |
4 | BAA02g11020 | A02 | 4971425 | G | A | missense_variant | MODERATE | c.406G>A|p.Glu136Lys |
S59 |
5 | BAA02g11020 | A02 | 4972655 | G | A | missense_variant | MODERATE | c.781G>A|p.Asp261Asn |
S155 S211 |
6 | BAA02g11020 | A02 | 4973089 | G | A | splice_region_variant&intron_variant | LOW | c.1047+5G>A| |
S223 |
7 | BAA02g11020 | A02 | 4973405 | G | A | missense_variant | MODERATE | c.1159G>A|p.Glu387Lys |
S295 |
8 | BAA02g11020 | A02 | 4973740 | C | T | missense_variant | MODERATE | c.1354C>T|p.Leu452Phe |
S71 |
9 | BAA02g11020 | A02 | 4974328 | C | T | downstream_gene_variant | MODIFIER | c.*3C>T| |
S58 |
10 | BAA02g11020 | A02 | 4975844 | C | T | downstream_gene_variant | MODIFIER | c.*1519C>T| |
S117 |