| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 34851 | BAA01g23380 | A01 | 12033164 | A | G | missense_variant | MODERATE | c.1618A>G|p.Thr540Ala |
S38 |
| 34852 | BAA01g23380 | A01 | 12033188 | G | A | missense_variant | MODERATE | c.1642G>A|p.Glu548Lys |
S172 S217 |
| 34853 | BAA01g23380 | A01 | 12034282 | C | T | downstream_gene_variant | MODIFIER | c.*407C>T| |
S264 |
| 34854 | BAA01g23380 | A01 | 12034877 | C | T | downstream_gene_variant | MODIFIER | c.*1002C>T| |
S16 |
| 34855 | BAA01g23380 | A01 | 12035992 | G | A | downstream_gene_variant | MODIFIER | c.*2117G>A| |
S238 |
| 34856 | BAA01g23390 | A01 | 12036426 | C | T | missense_variant | MODERATE | c.2401G>A|p.Asp801Asn |
S249 |
| 34857 | BAA01g23390 | A01 | 12036839 | C | T | missense_variant | MODERATE | c.2176G>A|p.Ala726Thr |
S107 |
| 34858 | BAA01g23390 | A01 | 12036860 | C | T | missense_variant | MODERATE | c.2155G>A|p.Glu719Lys |
S160 |
| 34859 | BAA01g23390 | A01 | 12038243 | G | A | synonymous_variant | LOW | c.1269C>T|p.Asn423Asn |
S140 |
| 34860 | BAA01g23390 | A01 | 12038317 | C | T | missense_variant | MODERATE | c.1195G>A|p.Asp399Asn |
S184 |
| 34861 | BAA01g23390 | A01 | 12038383 | C | T | missense_variant | MODERATE | c.1129G>A|p.Glu377Lys |
S167 |
| 34862 | BAA01g23390 | A01 | 12038417 | G | A | synonymous_variant | LOW | c.1095C>T|p.Asp365Asp |
S297 |
| 34863 | BAA01g23390 | A01 | 12038425 | G | A | stop_gained | HIGH | c.1087C>T|p.Arg363* |
S162 |
| 34864 | BAA01g23390 | A01 | 12038549 | G | A | synonymous_variant | LOW | c.963C>T|p.Phe321Phe |
S131 |
| 34865 | BAA01g23390 | A01 | 12038555 | C | T | synonymous_variant | LOW | c.957G>A|p.Glu319Glu |
S230 |
| 34866 | BAA01g23390 | A01 | 12038610 | C | T | missense_variant | MODERATE | c.902G>A|p.Gly301Glu |
S295 |
| 34867 | BAA01g23390 | A01 | 12039045 | G | A | synonymous_variant | LOW | c.616C>T|p.Leu206Leu |
S186 |
| 34868 | BAA01g23390 | A01 | 12039493 | C | T | intron_variant | MODIFIER | c.362+56G>A| |
S82 S92 |
| 34869 | BAA01g23390 | A01 | 12039503 | C | T | intron_variant | MODIFIER | c.362+46G>A| |
S171 |
| 34870 | BAA01g23390 | A01 | 12039563 | C | T | synonymous_variant | LOW | c.348G>A|p.Ala116Ala |
S55 |
| 34871 | BAA01g23390 | A01 | 12039806 | C | T | synonymous_variant | LOW | c.105G>A|p.Leu35Leu |
S183 |
| 34872 | BAA01g23390 | A01 | 12040223 | C | T | upstream_gene_variant | MODIFIER | c.-313G>A| |
S88 |
| 34873 | BAA01g23390 | A01 | 12040346 | C | A | upstream_gene_variant | MODIFIER | c.-436G>T| |
S232 S40 S6 S62 |
| 34874 | BAA01g23390 | A01 | 12041685 | G | A | upstream_gene_variant | MODIFIER | c.-1775C>T| |
S68 |
| 34875 | BAA01g23390 | A01 | 12041777 | C | T | upstream_gene_variant | MODIFIER | c.-1867G>A| |
S134 |