Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26780 | A01 | 15058293 | C | T | downstream_gene_variant | MODIFIER | c.*648G>A| |
S203 |
2 | BAA01g26780 | A01 | 15058489 | G | A | downstream_gene_variant | MODIFIER | c.*452C>T| |
S244 |
3 | BAA01g26780 | A01 | 15058539 | G | A | downstream_gene_variant | MODIFIER | c.*402C>T| |
S191 S235 |
4 | BAA01g26780 | A01 | 15058958 | C | T | missense_variant | MODERATE | c.721G>A|p.Val241Ile |
S275 |
5 | BAA01g26780 | A01 | 15059027 | C | T | missense_variant | MODERATE | c.652G>A|p.Asp218Asn |
S104 S52 |
6 | BAA01g26780 | A01 | 15059096 | C | T | missense_variant | MODERATE | c.583G>A|p.Gly195Arg |
S10 |
7 | BAA01g26780 | A01 | 15059164 | C | T | missense_variant | MODERATE | c.515G>A|p.Cys172Tyr |
S153 |
8 | BAA01g26780 | A01 | 15059591 | G | A | synonymous_variant | LOW | c.360C>T|p.Pro120Pro |
S126 |
9 | BAA01g26780 | A01 | 15059731 | G | A | missense_variant | MODERATE | c.220C>T|p.Pro74Ser |
S274 |
10 | BAA01g26780 | A01 | 15061425 | G | A | upstream_gene_variant | MODIFIER | c.-1388C>T| |
S74 |
11 | BAA01g26780 | A01 | 15061911 | C | T | upstream_gene_variant | MODIFIER | c.-1874G>A| |
S166 |
12 | BAA01g26780 | A01 | 15062282 | C | T | upstream_gene_variant | MODIFIER | c.-2245G>A| |
S114 |
13 | BAA01g26780 | A01 | 15062403 | C | T | upstream_gene_variant | MODIFIER | c.-2366G>A| |
S205 |
14 | BAA01g26780 | A01 | 15063201 | C | T | upstream_gene_variant | MODIFIER | c.-3164G>A| |
S4 |
15 | BAA01g26780 | A01 | 15063801 | T | A | upstream_gene_variant | MODIFIER | c.-3764A>T| |
S226 |
16 | BAA01g26780 | A01 | 15063862 | G | A | upstream_gene_variant | MODIFIER | c.-3825C>T| |
S240 |
17 | BAA01g26780 | A01 | 15064908 | G | A | upstream_gene_variant | MODIFIER | c.-4871C>T| |
S103 |