| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 104001 | BAA10g07860-BAA10g07870 | A10 | 4938879 | C | T | intergenic_region | MODIFIER | n.4938879C>T| |
S104 S52 |
| 104002 | BAA10g07860-BAA10g07870 | A10 | 4939301 | C | T | intergenic_region | MODIFIER | n.4939301C>T| |
S132 S137 S215 |
| 104003 | BAA10g07860-BAA10g07870 | A10 | 4939558 | C | T | intergenic_region | MODIFIER | n.4939558C>T| |
S224 |
| 104004 | BAA10g07860-BAA10g07870 | A10 | 4939619 | C | T | intergenic_region | MODIFIER | n.4939619C>T| |
S185 |
| 104005 | BAA10g07860-BAA10g07870 | A10 | 4940361 | G | A | intergenic_region | MODIFIER | n.4940361G>A| |
S157 S163 |
| 104006 | BAA10g07860-BAA10g07870 | A10 | 4940377 | G | A | intergenic_region | MODIFIER | n.4940377G>A| |
S18 |
| 104007 | BAA10g07860-BAA10g07870 | A10 | 4941370 | C | T | intergenic_region | MODIFIER | n.4941370C>T| |
S87 |
| 104008 | BAA10g07860-BAA10g07870 | A10 | 4941613 | C | T | intergenic_region | MODIFIER | n.4941613C>T| |
S130 |
| 104009 | BAA10g07860-BAA10g07870 | A10 | 4941799 | C | T | intergenic_region | MODIFIER | n.4941799C>T| |
S124 |
| 104010 | BAA10g07860-BAA10g07870 | A10 | 4941925 | C | T | intergenic_region | MODIFIER | n.4941925C>T| |
S235 |
| 104011 | BAA10g07860-BAA10g07870 | A10 | 4942436 | C | T | intergenic_region | MODIFIER | n.4942436C>T| |
S121 |
| 104012 | BAA10g07860-BAA10g07870 | A10 | 4942908 | G | A | intergenic_region | MODIFIER | n.4942908G>A| |
S36 |
| 104013 | BAA10g07860-BAA10g07870 | A10 | 4943472 | C | T | intergenic_region | MODIFIER | n.4943472C>T| |
S246 |
| 104014 | BAA10g07860-BAA10g07870 | A10 | 4943774 | C | T | intergenic_region | MODIFIER | n.4943774C>T| |
S238 |
| 104015 | BAA10g07860-BAA10g07870 | A10 | 4944662 | C | T | intergenic_region | MODIFIER | n.4944662C>T| |
S152 |
| 104016 | BAA10g07870 | A10 | 4946789 | T | C | upstream_gene_variant | MODIFIER | c.-3031T>C| |
S26 |
| 104017 | BAA10g07870 | A10 | 4949140 | C | T | upstream_gene_variant | MODIFIER | c.-680C>T| |
S139 |
| 104018 | BAA10g07880 | A10 | 4951463 | C | T | missense_variant | MODERATE | c.256C>T|p.Pro86Ser |
S135 |
| 104019 | BAA10g07870 | A10 | 4952845 | C | T | downstream_gene_variant | MODIFIER | c.*2588C>T| |
S259 |
| 104020 | BAA10g07870 | A10 | 4953073 | G | A | downstream_gene_variant | MODIFIER | c.*2816G>A| |
S180 |
| 104021 | BAA10g07870 | A10 | 4954012 | C | T | downstream_gene_variant | MODIFIER | c.*3755C>T| |
S67 |
| 104022 | BAA10g07870 | A10 | 4954525 | C | T | downstream_gene_variant | MODIFIER | c.*4268C>T| |
S183 |
| 104023 | BAA10g07870 | A10 | 4954634 | G | A | downstream_gene_variant | MODIFIER | c.*4377G>A| |
S262 |
| 104024 | BAA10g07880 | A10 | 4957177 | C | T | downstream_gene_variant | MODIFIER | c.*4224C>T| |
S108 |
| 104025 | BAA10g07880-BAA10g07890 | A10 | 4968039 | C | T | intergenic_region | MODIFIER | n.4968039C>T| |
S139 |