Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g45140 | A03 | 21556389 | G | A | downstream_gene_variant | MODIFIER | c.*2302C>T| |
S25 |
2 | BAA03g45140 | A03 | 21556445 | G | A | downstream_gene_variant | MODIFIER | c.*2246C>T| |
S276 |
3 | BAA03g45140 | A03 | 21556533 | C | T | downstream_gene_variant | MODIFIER | c.*2158G>A| |
S179 |
4 | BAA03g45140 | A03 | 21558130 | G | A | downstream_gene_variant | MODIFIER | c.*561C>T| |
S135 |
5 | BAA03g45140 | A03 | 21558868 | C | T | synonymous_variant | LOW | c.954G>A|p.Leu318Leu |
S1 S90 |
6 | BAA03g45140 | A03 | 21559011 | C | T | missense_variant | MODERATE | c.811G>A|p.Ala271Thr |
S200 |
7 | BAA03g45140 | A03 | 21559065 | G | A | missense_variant | MODERATE | c.757C>T|p.Leu253Phe |
S85 |
8 | BAA03g45140 | A03 | 21559460 | G | A | intron_variant | MODIFIER | c.421-59C>T| |
S124 |
9 | BAA03g45140 | A03 | 21560175 | C | T | intron_variant | MODIFIER | c.420+477G>A| |
S18 |
10 | BAA03g45140 | A03 | 21561147 | C | T | missense_variant | MODERATE | c.4G>A|p.Asp2Asn |
S9 |
11 | BAA03g45140 | A03 | 21561272 | G | A | upstream_gene_variant | MODIFIER | c.-122C>T| |
S177 |
12 | BAA03g45140 | A03 | 21561830 | C | T | upstream_gene_variant | MODIFIER | c.-680G>A| |
S67 |
13 | BAA03g45140 | A03 | 21562430 | G | A | upstream_gene_variant | MODIFIER | c.-1280C>T| |
S80 |
14 | BAA03g45140 | A03 | 21562896 | C | T | upstream_gene_variant | MODIFIER | c.-1746G>A| |
S131 |
15 | BAA03g45140 | A03 | 21563256 | G | A | upstream_gene_variant | MODIFIER | c.-2106C>T| |
S162 |
16 | BAA03g45140 | A03 | 21563478 | C | T | upstream_gene_variant | MODIFIER | c.-2328G>A| |
S121 |
17 | BAA03g45140 | A03 | 21563740 | G | A | upstream_gene_variant | MODIFIER | c.-2590C>T| |
S79 |
18 | BAA03g45140 | A03 | 21564054 | C | T | upstream_gene_variant | MODIFIER | c.-2904G>A| |
S187 |
19 | BAA03g45140 | A03 | 21564302 | G | A | upstream_gene_variant | MODIFIER | c.-3152C>T| |
S186 |