Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g34260 | A03 | 15886302 | G | A | upstream_gene_variant | MODIFIER | c.-3656G>A| |
S296 |
2 | BAA03g34260 | A03 | 15886804 | T | A | upstream_gene_variant | MODIFIER | c.-3154T>A| |
S281 |
3 | BAA03g34260 | A03 | 15888179 | C | T | upstream_gene_variant | MODIFIER | c.-1779C>T| |
S159 S243 |
4 | BAA03g34260 | A03 | 15888581 | G | A | upstream_gene_variant | MODIFIER | c.-1377G>A| |
S267 |
5 | BAA03g34260 | A03 | 15889102 | C | T | upstream_gene_variant | MODIFIER | c.-856C>T| |
S262 |
6 | BAA03g34260 | A03 | 15889274 | C | T | upstream_gene_variant | MODIFIER | c.-684C>T| |
S176 |
7 | BAA03g34260 | A03 | 15889290 | C | T | upstream_gene_variant | MODIFIER | c.-668C>T| |
S34 S4 S6 |
8 | BAA03g34260 | A03 | 15890711 | C | T | missense_variant | MODERATE | c.517C>T|p.Pro173Ser |
S241 |
9 | BAA03g34260 | A03 | 15890873 | G | A | synonymous_variant | LOW | c.597G>A|p.Arg199Arg |
S45 |
10 | BAA03g34260 | A03 | 15891131 | C | T | missense_variant | MODERATE | c.770C>T|p.Ala257Val |
S294 |
11 | BAA03g34260 | A03 | 15891362 | G | A | intron_variant | MODIFIER | c.934-50G>A| |
S23 |
12 | BAA03g34260 | A03 | 15891460 | G | A | missense_variant | MODERATE | c.982G>A|p.Glu328Lys |
S60 |
13 | BAA03g34260 | A03 | 15892394 | C | T | synonymous_variant | LOW | c.1474C>T|p.Leu492Leu |
S134 |
14 | BAA03g34260 | A03 | 15892406 | C | T | missense_variant | MODERATE | c.1486C>T|p.Leu496Phe |
S182 |
15 | BAA03g34260 | A03 | 15892961 | G | A | intron_variant | MODIFIER | c.1682-204G>A| |
S107 |
16 | BAA03g34260 | A03 | 15895652 | C | T | intron_variant | MODIFIER | c.3074+33C>T| |
S150 |
17 | BAA03g34260 | A03 | 15898995 | G | A | missense_variant | MODERATE | c.5086G>A|p.Glu1696Lys |
S245 |
18 | BAA03g34260 | A03 | 15899437 | C | T | missense_variant | MODERATE | c.5528C>T|p.Ser1843Phe |
S264 |
19 | BAA03g34260 | A03 | 15899782 | C | T | missense_variant | MODERATE | c.5785C>T|p.Pro1929Ser |
S153 |
20 | BAA03g34260 | A03 | 15900204 | C | T | missense_variant | MODERATE | c.6119C>T|p.Ser2040Leu |
S105 S106 |