| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 198451 | BAA02g29750 | A02 | 17082838 | G | A | upstream_gene_variant | MODIFIER | c.-1155C>T| |
S48 |
| 198452 | BAA02g29750 | A02 | 17082871 | G | A | upstream_gene_variant | MODIFIER | c.-1188C>T| |
S281 |
| 198453 | BAA02g29750 | A02 | 17083336 | G | A | upstream_gene_variant | MODIFIER | c.-1653C>T| |
S302 |
| 198454 | BAA02g29750 | A02 | 17083566 | G | A | upstream_gene_variant | MODIFIER | c.-1883C>T| |
S18 S294 S36 |
| 198455 | BAA02g29750 | A02 | 17083788 | C | T | upstream_gene_variant | MODIFIER | c.-2105G>A| |
S8 |
| 198456 | BAA02g29750 | A02 | 17084054 | G | A | upstream_gene_variant | MODIFIER | c.-2371C>T| |
S23 |
| 198457 | BAA02g29750 | A02 | 17084086 | G | A | upstream_gene_variant | MODIFIER | c.-2403C>T| |
S17 |
| 198458 | BAA02g29760 | A02 | 17086741 | C | T | missense_variant | MODERATE | c.532G>A|p.Gly178Ser |
S183 S198 |
| 198459 | BAA02g29760 | A02 | 17086764 | G | A | missense_variant | MODERATE | c.509C>T|p.Ser170Phe |
S297 |
| 198460 | BAA02g29760 | A02 | 17086780 | G | A | missense_variant | MODERATE | c.493C>T|p.Leu165Phe |
S72 S78 |
| 198461 | BAA02g29760 | A02 | 17086790 | G | A | synonymous_variant | LOW | c.483C>T|p.Phe161Phe |
S133 |
| 198462 | BAA02g29760 | A02 | 17087073 | C | T | intron_variant | MODIFIER | c.230-30G>A| |
S54 |
| 198463 | BAA02g29760 | A02 | 17087327 | C | T | intron_variant | MODIFIER | c.230-284G>A| |
S53 |
| 198464 | BAA02g29760 | A02 | 17087447 | C | T | intron_variant | MODIFIER | c.229+202G>A| |
S203 |
| 198465 | BAA02g29760 | A02 | 17088004 | C | T | upstream_gene_variant | MODIFIER | c.-127G>A| |
S117 |
| 198466 | BAA02g29760 | A02 | 17088359 | G | A | upstream_gene_variant | MODIFIER | c.-482C>T| |
S50 |
| 198467 | BAA02g29760 | A02 | 17088618 | G | A | upstream_gene_variant | MODIFIER | c.-741C>T| |
S197 |
| 198468 | BAA02g29760 | A02 | 17089854 | G | A | upstream_gene_variant | MODIFIER | c.-1977C>T| |
S116 |
| 198469 | BAA02g29760 | A02 | 17089897 | C | T | upstream_gene_variant | MODIFIER | c.-2020G>A| |
S216 |
| 198470 | BAA02g29760 | A02 | 17092032 | G | A | upstream_gene_variant | MODIFIER | c.-4155C>T| |
S155 S211 |
| 198471 | BAA02g29760 | A02 | 17092212 | G | A | upstream_gene_variant | MODIFIER | c.-4335C>T| |
S291 |
| 198472 | BAA02g29760-BAA02g29770 | A02 | 17093284 | C | T | intergenic_region | MODIFIER | n.17093284C>T| |
S231 |
| 198473 | BAA02g29760-BAA02g29770 | A02 | 17094467 | C | T | intergenic_region | MODIFIER | n.17094467C>T| |
S226 |
| 198474 | BAA02g29760-BAA02g29770 | A02 | 17094940 | C | T | intergenic_region | MODIFIER | n.17094940C>T| |
S76 |
| 198475 | BAA02g29760-BAA02g29770 | A02 | 17097709 | A | C | intergenic_region | MODIFIER | n.17097709A>C| |
S150 S172 S202 |