| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 178601 | BAA02g19450 | A02 | 10102707 | G | A | downstream_gene_variant | MODIFIER | c.*3661G>A| |
S289 S290 |
| 178602 | BAA02g19470 | A02 | 10102776 | C | T | missense_variant | MODERATE | c.257C>T|p.Thr86Ile |
S167 |
| 178603 | BAA02g19450 | A02 | 10102939 | G | A | downstream_gene_variant | MODIFIER | c.*3893G>A| |
S126 |
| 178604 | BAA02g19450 | A02 | 10103725 | G | A | downstream_gene_variant | MODIFIER | c.*4679G>A| |
S34 |
| 178605 | BAA02g19450 | A02 | 10103727 | G | A | downstream_gene_variant | MODIFIER | c.*4681G>A| |
S213 |
| 178606 | BAA02g19460 | A02 | 10104077 | G | A | downstream_gene_variant | MODIFIER | c.*2888G>A| |
S57 |
| 178607 | BAA02g19460 | A02 | 10104561 | C | T | downstream_gene_variant | MODIFIER | c.*3372C>T| |
S182 |
| 178608 | BAA02g19460 | A02 | 10104799 | C | T | downstream_gene_variant | MODIFIER | c.*3610C>T| |
S283 |
| 178609 | BAA02g19480 | A02 | 10105070 | G | A | missense_variant | MODERATE | c.368C>T|p.Ser123Phe |
S297 |
| 178610 | BAA02g19480 | A02 | 10105278 | G | A | missense_variant | MODERATE | c.160C>T|p.Pro54Ser |
S61 |
| 178611 | BAA02g19480 | A02 | 10105984 | C | T | upstream_gene_variant | MODIFIER | c.-547G>A| |
S88 |
| 178612 | BAA02g19480 | A02 | 10106708 | G | A | upstream_gene_variant | MODIFIER | c.-1271C>T| |
S137 S215 |
| 178613 | BAA02g19480 | A02 | 10107059 | C | T | upstream_gene_variant | MODIFIER | c.-1622G>A| |
S180 |
| 178614 | BAA02g19480 | A02 | 10108158 | G | A | upstream_gene_variant | MODIFIER | c.-2721C>T| |
S41 |
| 178615 | BAA02g19480 | A02 | 10109696 | C | T | upstream_gene_variant | MODIFIER | c.-4259G>A| |
S80 |
| 178616 | BAA02g19480-BAA02g19490 | A02 | 10111066 | C | T | intergenic_region | MODIFIER | n.10111066C>T| |
S100 |
| 178617 | BAA02g19480-BAA02g19490 | A02 | 10111122 | C | T | intergenic_region | MODIFIER | n.10111122C>T| |
S97 |
| 178618 | BAA02g19490 | A02 | 10112484 | C | T | upstream_gene_variant | MODIFIER | c.-4082C>T| |
S44 |
| 178619 | BAA02g19490 | A02 | 10112764 | C | T | upstream_gene_variant | MODIFIER | c.-3802C>T| |
S183 S198 |
| 178620 | BAA02g19490 | A02 | 10112841 | C | T | upstream_gene_variant | MODIFIER | c.-3725C>T| |
S179 |
| 178621 | BAA02g19490 | A02 | 10113254 | G | A | upstream_gene_variant | MODIFIER | c.-3312G>A| |
S303 |
| 178622 | BAA02g19490 | A02 | 10113894 | C | T | upstream_gene_variant | MODIFIER | c.-2672C>T| |
S211 S227 |
| 178623 | BAA02g19490 | A02 | 10114005 | C | T | upstream_gene_variant | MODIFIER | c.-2561C>T| |
S142 |
| 178624 | BAA02g19490 | A02 | 10114310 | C | T | upstream_gene_variant | MODIFIER | c.-2256C>T| |
S100 |
| 178625 | BAA02g19490 | A02 | 10114389 | C | T | upstream_gene_variant | MODIFIER | c.-2177C>T| |
S209 |