Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g59820 | A03 | 30056120 | G | A | upstream_gene_variant | MODIFIER | c.-4519G>A| |
S224 |
2 | BAA03g59820 | A03 | 30056380 | G | A | upstream_gene_variant | MODIFIER | c.-4259G>A| |
S268 |
3 | BAA03g59820 | A03 | 30056446 | C | T | upstream_gene_variant | MODIFIER | c.-4193C>T| |
S202 |
4 | BAA03g59820 | A03 | 30057172 | C | T | upstream_gene_variant | MODIFIER | c.-3467C>T| |
S203 S301 |
5 | BAA03g59820 | A03 | 30057719 | C | T | upstream_gene_variant | MODIFIER | c.-2920C>T| |
S244 |
6 | BAA03g59820 | A03 | 30058031 | G | A | upstream_gene_variant | MODIFIER | c.-2608G>A| |
S242 |
7 | BAA03g59820 | A03 | 30058056 | G | A | upstream_gene_variant | MODIFIER | c.-2583G>A| |
S146 |
8 | BAA03g59820 | A03 | 30059441 | C | T | upstream_gene_variant | MODIFIER | c.-1198C>T| |
S174 |
9 | BAA03g59820 | A03 | 30060010 | C | T | upstream_gene_variant | MODIFIER | c.-629C>T| |
S139 |
10 | BAA03g59820 | A03 | 30061225 | C | T | intron_variant | MODIFIER | c.273+221C>T| |
S216 |
11 | BAA03g59820 | A03 | 30062025 | G | A | intron_variant | MODIFIER | c.420-15G>A| |
S171 |
12 | BAA03g59820 | A03 | 30062268 | C | T | intron_variant | MODIFIER | c.576+72C>T| |
S211 |
13 | BAA03g59820 | A03 | 30062820 | G | A | intron_variant | MODIFIER | c.636-137G>A| |
S68 |
14 | BAA03g59820 | A03 | 30064378 | G | A | missense_variant | MODERATE | c.1408G>A|p.Asp470Asn |
S95 |
15 | BAA03g59820 | A03 | 30064534 | C | T | intron_variant | MODIFIER | c.1488+76C>T| |
S172 |
16 | BAA03g59820 | A03 | 30064791 | G | A | intron_variant | MODIFIER | c.1489-290G>A| |
S284 |
17 | BAA03g59820 | A03 | 30064893 | G | A | intron_variant | MODIFIER | c.1489-188G>A| |
S284 |
18 | BAA03g59820 | A03 | 30065130 | C | T | intron_variant | MODIFIER | c.1526+12C>T| |
S243 |
19 | BAA03g59820 | A03 | 30065712 | C | T | synonymous_variant | LOW | c.1845C>T|p.Leu615Leu |
S116 |
20 | BAA03g59820 | A03 | 30066129 | C | T | intron_variant | MODIFIER | c.1960-160C>T| |
S165 |
21 | BAA03g59820 | A03 | 30066748 | G | A | intron_variant | MODIFIER | c.2130+48G>A| |
S169 |
22 | BAA03g59820 | A03 | 30068072 | G | A | missense_variant | MODERATE | c.2851G>A|p.Ala951Thr |
S123 |
23 | BAA03g59820 | A03 | 30068274 | C | T | intron_variant | MODIFIER | c.2955+98C>T| |
S263 |
24 | BAA03g59820 | A03 | 30068334 | C | T | intron_variant | MODIFIER | c.2955+158C>T| |
S161 |
25 | BAA03g59820 | A03 | 30072523 | C | T | missense_variant | MODERATE | c.4522C>T|p.Leu1508Phe |
S42 |