| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 56351 | BAA01g30600 | A01 | 19572988 | G | A | missense_variant | MODERATE | c.220G>A|p.Val74Ile |
S288 |
| 56352 | BAA01g30600 | A01 | 19573201 | G | A | missense_variant | MODERATE | c.433G>A|p.Asp145Asn |
S194 |
| 56353 | BAA01g30590 | A01 | 19573392 | G | A | downstream_gene_variant | MODIFIER | c.*1418G>A| |
S209 |
| 56354 | BAA01g30590 | A01 | 19573421 | C | T | downstream_gene_variant | MODIFIER | c.*1447C>T| |
S44 |
| 56355 | BAA01g30590 | A01 | 19573820 | G | A | downstream_gene_variant | MODIFIER | c.*1846G>A| |
S187 |
| 56356 | BAA01g30600 | A01 | 19577387 | G | A | downstream_gene_variant | MODIFIER | c.*4172G>A| |
S103 |
| 56357 | BAA01g30600 | A01 | 19577519 | G | A | downstream_gene_variant | MODIFIER | c.*4304G>A| |
S281 |
| 56358 | BAA01g30610 | A01 | 19577573 | C | T | missense_variant | MODERATE | c.1237G>A|p.Ala413Thr |
S303 |
| 56359 | BAA01g30610 | A01 | 19578135 | C | T | missense_variant | MODERATE | c.757G>A|p.Gly253Arg |
S76 |
| 56360 | BAA01g30610 | A01 | 19581106 | C | T | upstream_gene_variant | MODIFIER | c.-1887G>A| |
S54 |
| 56361 | BAA01g30610 | A01 | 19581109 | C | T | upstream_gene_variant | MODIFIER | c.-1890G>A| |
S170 |
| 56362 | BAA01g30620 | A01 | 19586008 | G | A | downstream_gene_variant | MODIFIER | c.*4766C>T| |
S7 |
| 56363 | BAA01g30620 | A01 | 19586048 | C | T | downstream_gene_variant | MODIFIER | c.*4726G>A| |
S69 |
| 56364 | BAA01g30620 | A01 | 19587274 | G | A | downstream_gene_variant | MODIFIER | c.*3500C>T| |
S232 |
| 56365 | BAA01g30620 | A01 | 19587855 | C | T | downstream_gene_variant | MODIFIER | c.*2919G>A| |
S270 |
| 56366 | BAA01g30620 | A01 | 19588625 | G | A | downstream_gene_variant | MODIFIER | c.*2149C>T| |
S8 |
| 56367 | BAA01g30620 | A01 | 19588818 | C | T | downstream_gene_variant | MODIFIER | c.*1956G>A| |
S206 S26 |
| 56368 | BAA01g30620 | A01 | 19589113 | C | T | downstream_gene_variant | MODIFIER | c.*1661G>A| |
S48 |
| 56369 | BAA01g30620 | A01 | 19589564 | G | A | downstream_gene_variant | MODIFIER | c.*1210C>T| |
S297 |
| 56370 | BAA01g30620 | A01 | 19591216 | C | T | intron_variant | MODIFIER | c.1378-47G>A| |
S270 |
| 56371 | BAA01g30620 | A01 | 19591377 | C | T | intron_variant | MODIFIER | c.1330-22G>A| |
S113 |
| 56372 | BAA01g30620 | A01 | 19591773 | C | T | missense_variant | MODERATE | c.1145G>A|p.Arg382Lys |
S115 |
| 56373 | BAA01g30620 | A01 | 19593085 | C | T | synonymous_variant | LOW | c.414G>A|p.Lys138Lys |
S177 |
| 56374 | BAA01g30620 | A01 | 19593556 | G | A | missense_variant | MODERATE | c.97C>T|p.Pro33Ser |
S238 |
| 56375 | BAA01g30620 | A01 | 19594248 | G | A | upstream_gene_variant | MODIFIER | c.-596C>T| |
S105 S106 |