Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g15950 | A09 | 9174424 | C | T | upstream_gene_variant | MODIFIER | c.-4937C>T| |
S263 |
2 | BAA09g15950 | A09 | 9174723 | G | A | upstream_gene_variant | MODIFIER | c.-4638G>A| |
S180 |
3 | BAA09g15950 | A09 | 9174887 | C | T | upstream_gene_variant | MODIFIER | c.-4474C>T| |
S295 |
4 | BAA09g15950 | A09 | 9174962 | C | T | upstream_gene_variant | MODIFIER | c.-4399C>T| |
S156 |
5 | BAA09g15950 | A09 | 9176439 | G | A | upstream_gene_variant | MODIFIER | c.-2922G>A| |
S197 |
6 | BAA09g15950 | A09 | 9176764 | G | A | upstream_gene_variant | MODIFIER | c.-2597G>A| |
S169 |
7 | BAA09g15950 | A09 | 9179802 | G | A | intron_variant | MODIFIER | c.235-27G>A| |
S233 |
8 | BAA09g15950 | A09 | 9179828 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.235-1G>A| |
S184 |
9 | BAA09g15950 | A09 | 9180994 | C | T | missense_variant | MODERATE | c.739C>T|p.Leu247Phe |
S186 |
10 | BAA09g15950 | A09 | 9181285 | G | A | intron_variant | MODIFIER | c.852+86G>A| |
S203 |
11 | BAA09g15950 | A09 | 9184286 | G | A | synonymous_variant | LOW | c.2793G>A|p.Glu931Glu |
S4 |
12 | BAA09g15950 | A09 | 9184395 | C | T | missense_variant | MODERATE | c.2902C>T|p.Leu968Phe |
S128 |
13 | BAA09g15950 | A09 | 9185115 | G | A | downstream_gene_variant | MODIFIER | c.*183G>A| |
S89 |
14 | BAA09g15950 | A09 | 9185118 | G | A | downstream_gene_variant | MODIFIER | c.*186G>A| |
S193 |
15 | BAA09g15950 | A09 | 9185844 | C | T | downstream_gene_variant | MODIFIER | c.*912C>T| |
S168 |