| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 195351 | BAA02g28470 | A02 | 16014380 | G | A | upstream_gene_variant | MODIFIER | c.-4592C>T| |
S28 |
| 195352 | BAA02g28480 | A02 | 16014812 | G | A | upstream_gene_variant | MODIFIER | c.-1562C>T| |
S297 |
| 195353 | BAA02g28490 | A02 | 16016050 | G | A | stop_gained | HIGH | c.318G>A|p.Trp106* |
S217 S248 |
| 195354 | BAA02g28490 | A02 | 16016122 | C | T | synonymous_variant | LOW | c.390C>T|p.Ala130Ala |
S296 |
| 195355 | BAA02g28490 | A02 | 16017010 | G | A | synonymous_variant | LOW | c.1053G>A|p.Gln351Gln |
S256 |
| 195356 | BAA02g28490 | A02 | 16017249 | G | A | missense_variant | MODERATE | c.1292G>A|p.Arg431Lys |
S247 |
| 195357 | BAA02g28480 | A02 | 16017819 | G | A | upstream_gene_variant | MODIFIER | c.-4569C>T| |
S130 |
| 195358 | BAA02g28480 | A02 | 16017910 | G | A | upstream_gene_variant | MODIFIER | c.-4660C>T| |
S161 |
| 195359 | BAA02g28480 | A02 | 16018006 | C | T | upstream_gene_variant | MODIFIER | c.-4756G>A| |
S177 |
| 195360 | BAA02g28500 | A02 | 16019180 | G | A | synonymous_variant | LOW | c.474G>A|p.Glu158Glu |
S187 |
| 195361 | BAA02g28500 | A02 | 16019274 | G | A | missense_variant | MODERATE | c.568G>A|p.Val190Ile |
S278 |
| 195362 | BAA02g28500 | A02 | 16019724 | C | T | missense_variant | MODERATE | c.1018C>T|p.Pro340Ser |
S266 |
| 195363 | BAA02g28500 | A02 | 16019725 | C | T | missense_variant | MODERATE | c.1019C>T|p.Pro340Leu |
S277 |
| 195364 | BAA02g28510 | A02 | 16021379 | G | A | missense_variant | MODERATE | c.604G>A|p.Asp202Asn |
S202 |
| 195365 | BAA02g28510 | A02 | 16022211 | C | T | missense_variant | MODERATE | c.1436C>T|p.Pro479Leu |
S268 |
| 195366 | BAA02g28520 | A02 | 16022264 | G | A | missense_variant | MODERATE | c.28G>A|p.Gly10Ser |
S50 |
| 195367 | BAA02g28520 | A02 | 16022573 | G | A | missense_variant | MODERATE | c.337G>A|p.Glu113Lys |
S28 |
| 195368 | BAA02g28520 | A02 | 16022918 | C | T | synonymous_variant | LOW | c.682C>T|p.Leu228Leu |
S293 |
| 195369 | BAA02g28520 | A02 | 16023641 | G | A | missense_variant | MODERATE | c.1405G>A|p.Val469Met |
S168 |
| 195370 | BAA02g28520 | A02 | 16023793 | C | T | synonymous_variant | LOW | c.1557C>T|p.Ile519Ile |
S64 |
| 195371 | BAA02g28520 | A02 | 16024264 | G | A | synonymous_variant | LOW | c.2028G>A|p.Pro676Pro |
S35 |
| 195372 | BAA02g28520 | A02 | 16024472 | G | A | missense_variant | MODERATE | c.2236G>A|p.Glu746Lys |
S149 |
| 195373 | BAA02g28520 | A02 | 16025177 | G | A | missense_variant | MODERATE | c.2941G>A|p.Asp981Asn |
S97 |
| 195374 | BAA02g28510 | A02 | 16026449 | G | A | downstream_gene_variant | MODIFIER | c.*4213G>A| |
S99 |
| 195375 | BAA02g28510 | A02 | 16026610 | C | T | downstream_gene_variant | MODIFIER | c.*4374C>T| |
S244 |