| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 101551 | BAA10g07250 | A10 | 4086896 | G | A | upstream_gene_variant | MODIFIER | c.-2711G>A| |
S164 |
| 101552 | BAA10g07250 | A10 | 4087090 | C | T | upstream_gene_variant | MODIFIER | c.-2517C>T| |
S244 |
| 101553 | BAA10g07250 | A10 | 4090138 | G | A | missense_variant | MODERATE | c.233G>A|p.Gly78Glu |
S255 |
| 101554 | BAA10g07250 | A10 | 4090388 | C | T | downstream_gene_variant | MODIFIER | c.*180C>T| |
S193 |
| 101555 | BAA10g07250 | A10 | 4090436 | G | A | downstream_gene_variant | MODIFIER | c.*228G>A| |
S215 |
| 101556 | BAA10g07250 | A10 | 4090680 | G | A | downstream_gene_variant | MODIFIER | c.*472G>A| |
S172 |
| 101557 | BAA10g07250 | A10 | 4090930 | C | T | downstream_gene_variant | MODIFIER | c.*722C>T| |
S263 |
| 101558 | BAA10g07250 | A10 | 4091768 | C | T | downstream_gene_variant | MODIFIER | c.*1560C>T| |
S249 |
| 101559 | BAA10g07250 | A10 | 4091920 | G | A | downstream_gene_variant | MODIFIER | c.*1712G>A| |
S198 |
| 101560 | BAA10g07250 | A10 | 4092240 | C | T | downstream_gene_variant | MODIFIER | c.*2032C>T| |
S263 |
| 101561 | BAA10g07250 | A10 | 4093037 | C | T | downstream_gene_variant | MODIFIER | c.*2829C>T| |
S11 |
| 101562 | BAA10g07250 | A10 | 4093232 | G | A | downstream_gene_variant | MODIFIER | c.*3024G>A| |
S241 |
| 101563 | BAA10g07250 | A10 | 4093309 | G | A | downstream_gene_variant | MODIFIER | c.*3101G>A| |
S302 |
| 101564 | BAA10g07250 | A10 | 4093352 | G | A | downstream_gene_variant | MODIFIER | c.*3144G>A| |
S280 |
| 101565 | BAA10g07250 | A10 | 4093779 | G | A | downstream_gene_variant | MODIFIER | c.*3571G>A| |
S178 |
| 101566 | BAA10g07250 | A10 | 4094228 | G | A | downstream_gene_variant | MODIFIER | c.*4020G>A| |
S139 |
| 101567 | BAA10g07250 | A10 | 4094388 | C | T | downstream_gene_variant | MODIFIER | c.*4180C>T| |
S282 |
| 101568 | BAA10g07250 | A10 | 4094611 | C | T | downstream_gene_variant | MODIFIER | c.*4403C>T| |
S6 |
| 101569 | BAA10g07250-BAA10g07260 | A10 | 4095446 | C | T | intergenic_region | MODIFIER | n.4095446C>T| |
S206 S26 |
| 101570 | BAA10g07250-BAA10g07260 | A10 | 4095785 | C | T | intergenic_region | MODIFIER | n.4095785C>T| |
S282 |
| 101571 | BAA10g07250-BAA10g07260 | A10 | 4095944 | G | A | intergenic_region | MODIFIER | n.4095944G>A| |
S67 |
| 101572 | BAA10g07250-BAA10g07260 | A10 | 4096352 | G | A | intergenic_region | MODIFIER | n.4096352G>A| |
S156 |
| 101573 | BAA10g07250-BAA10g07260 | A10 | 4097580 | G | A | intergenic_region | MODIFIER | n.4097580G>A| |
S112 |
| 101574 | BAA10g07250-BAA10g07260 | A10 | 4097643 | G | A | intergenic_region | MODIFIER | n.4097643G>A| |
S296 |
| 101575 | BAA10g07250-BAA10g07260 | A10 | 4098435 | C | T | intergenic_region | MODIFIER | n.4098435C>T| |
S181 |