Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18890 | A01 | 9279181 | G | A | missense_variant | MODERATE | c.1751C>T|p.Ala584Val |
S203 |
2 | BAA01g18890 | A01 | 9279248 | C | T | missense_variant | MODERATE | c.1684G>A|p.Ala562Thr |
S136 |
3 | BAA01g18890 | A01 | 9279755 | G | A | missense_variant | MODERATE | c.1177C>T|p.Arg393Trp |
S275 |
4 | BAA01g18890 | A01 | 9280968 | G | A | missense_variant | MODERATE | c.82C>T|p.Pro28Ser |
S87 |
5 | BAA01g18890 | A01 | 9281017 | C | T | synonymous_variant | LOW | c.33G>A|p.Val11Val |
S118 |
6 | BAA01g18890 | A01 | 9281096 | G | A | upstream_gene_variant | MODIFIER | c.-47C>T| |
S249 |
7 | BAA01g18890 | A01 | 9281206 | G | A | upstream_gene_variant | MODIFIER | c.-157C>T| |
S293 |
8 | BAA01g18890 | A01 | 9281322 | C | T | upstream_gene_variant | MODIFIER | c.-273G>A| |
S153 |
9 | BAA01g18890 | A01 | 9281992 | C | T | upstream_gene_variant | MODIFIER | c.-943G>A| |
S112 |
10 | BAA01g18890 | A01 | 9282470 | C | T | upstream_gene_variant | MODIFIER | c.-1421G>A| |
S210 S225 |
11 | BAA01g18890 | A01 | 9282621 | C | T | upstream_gene_variant | MODIFIER | c.-1572G>A| |
S16 |
12 | BAA01g18890 | A01 | 9284114 | C | T | upstream_gene_variant | MODIFIER | c.-3065G>A| |
S160 |