| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 99651 | BAA10g06620 | A10 | 3479023 | G | A | missense_variant | MODERATE | c.53C>T|p.Ala18Val |
S15 |
| 99652 | BAA10g06620 | A10 | 3479843 | C | T | upstream_gene_variant | MODIFIER | c.-768G>A| |
S68 |
| 99653 | BAA10g06620 | A10 | 3480236 | G | A | upstream_gene_variant | MODIFIER | c.-1161C>T| |
S283 |
| 99654 | BAA10g06620 | A10 | 3480321 | C | T | upstream_gene_variant | MODIFIER | c.-1246G>A| |
S61 |
| 99655 | BAA10g06620 | A10 | 3480970 | A | T | upstream_gene_variant | MODIFIER | c.-1895T>A| |
S157 S163 |
| 99656 | BAA10g06620 | A10 | 3481787 | G | A | upstream_gene_variant | MODIFIER | c.-2712C>T| |
S262 |
| 99657 | BAA10g06620 | A10 | 3481974 | G | A | upstream_gene_variant | MODIFIER | c.-2899C>T| |
S39 |
| 99658 | BAA10g06620 | A10 | 3482607 | G | A | upstream_gene_variant | MODIFIER | c.-3532C>T| |
S107 |
| 99659 | BAA10g06620 | A10 | 3483261 | C | T | upstream_gene_variant | MODIFIER | c.-4186G>A| |
S204 |
| 99660 | BAA10g06620-BAA10g06630 | A10 | 3485004 | C | T | intergenic_region | MODIFIER | n.3485004C>T| |
S275 |
| 99661 | BAA10g06620-BAA10g06630 | A10 | 3490677 | C | T | intergenic_region | MODIFIER | n.3490677C>T| |
S81 S85 |
| 99662 | BAA10g06620-BAA10g06630 | A10 | 3490782 | G | A | intergenic_region | MODIFIER | n.3490782G>A| |
S302 |
| 99663 | BAA10g06630 | A10 | 3491668 | G | A | downstream_gene_variant | MODIFIER | c.*4874C>T| |
S192 |
| 99664 | BAA10g06630 | A10 | 3494239 | G | A | downstream_gene_variant | MODIFIER | c.*2303C>T| |
S295 |
| 99665 | BAA10g06630 | A10 | 3496858 | G | A | missense_variant | MODERATE | c.1303C>T|p.Leu435Phe |
S45 |
| 99666 | BAA10g06630 | A10 | 3497505 | G | A | intron_variant | MODIFIER | c.899+23C>T| |
S279 |
| 99667 | BAA10g06630 | A10 | 3498215 | G | A | missense_variant | MODERATE | c.394C>T|p.Leu132Phe |
S172 S217 |
| 99668 | BAA10g06630 | A10 | 3498942 | C | T | intron_variant | MODIFIER | c.271-604G>A| |
S155 S211 |
| 99669 | BAA10g06630 | A10 | 3499691 | C | T | intron_variant | MODIFIER | c.270+734G>A| |
S276 |
| 99670 | BAA10g06630 | A10 | 3499792 | G | A | intron_variant | MODIFIER | c.270+633C>T| |
S184 |
| 99671 | BAA10g06630 | A10 | 3501376 | G | A | upstream_gene_variant | MODIFIER | c.-682C>T| |
S12 |
| 99672 | BAA10g06630 | A10 | 3501794 | C | T | upstream_gene_variant | MODIFIER | c.-1100G>A| |
S35 |
| 99673 | BAA10g06630 | A10 | 3501861 | G | A | upstream_gene_variant | MODIFIER | c.-1167C>T| |
S292 |
| 99674 | BAA10g06630 | A10 | 3503311 | C | T | upstream_gene_variant | MODIFIER | c.-2617G>A| |
S287 |
| 99675 | BAA10g06630 | A10 | 3503546 | G | A | upstream_gene_variant | MODIFIER | c.-2852C>T| |
S4 |