Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38650 | A09 | 46408852 | G | A | downstream_gene_variant | MODIFIER | c.*656C>T| |
S112 |
2 | BAA09g38650 | A09 | 46409061 | C | T | downstream_gene_variant | MODIFIER | c.*447G>A| |
S61 |
3 | BAA09g38650 | A09 | 46409646 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1012-1G>A| |
S286 |
4 | BAA09g38650 | A09 | 46409997 | G | A | missense_variant | MODERATE | c.850C>T|p.Leu284Phe |
S203 |
5 | BAA09g38650 | A09 | 46410530 | G | A | missense_variant | MODERATE | c.482C>T|p.Pro161Leu |
S200 |
6 | BAA09g38650 | A09 | 46410646 | C | T | synonymous_variant | LOW | c.366G>A|p.Gln122Gln |
S149 |
7 | BAA09g38650 | A09 | 46411723 | C | T | upstream_gene_variant | MODIFIER | c.-463G>A| |
S279 |
8 | BAA09g38650 | A09 | 46412560 | G | A | upstream_gene_variant | MODIFIER | c.-1300C>T| |
S295 |
9 | BAA09g38650 | A09 | 46413179 | C | T | upstream_gene_variant | MODIFIER | c.-1919G>A| |
S256 |
10 | BAA09g38650 | A09 | 46413229 | G | A | upstream_gene_variant | MODIFIER | c.-1969C>T| |
S177 |
11 | BAA09g38650 | A09 | 46413806 | C | T | upstream_gene_variant | MODIFIER | c.-2546G>A| |
S260 |
12 | BAA09g38650 | A09 | 46413953 | G | A | upstream_gene_variant | MODIFIER | c.-2693C>T| |
S270 |
13 | BAA09g38650 | A09 | 46414154 | G | A | upstream_gene_variant | MODIFIER | c.-2894C>T| |
S62 |
14 | BAA09g38650 | A09 | 46414802 | C | T | upstream_gene_variant | MODIFIER | c.-3542G>A| |
S232 |
15 | BAA09g38650 | A09 | 46416103 | G | A | upstream_gene_variant | MODIFIER | c.-4843C>T| |
S174 S27 |