| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 132551 | BAA10g19430 | A10 | 17814767 | G | A | intron_variant | MODIFIER | c.384+37C>T| |
S28 |
| 132552 | BAA10g19430 | A10 | 17814839 | C | T | missense_variant | MODERATE | c.349G>A|p.Gly117Arg |
S18 |
| 132553 | BAA10g19430 | A10 | 17814972 | C | T | missense_variant | MODERATE | c.280G>A|p.Ala94Thr |
S18 |
| 132554 | BAA10g19430 | A10 | 17815786 | G | A | upstream_gene_variant | MODIFIER | c.-231C>T| |
S289 S290 |
| 132555 | BAA10g19430 | A10 | 17816840 | G | A | upstream_gene_variant | MODIFIER | c.-1285C>T| |
S261 |
| 132556 | BAA10g19430 | A10 | 17819101 | C | T | upstream_gene_variant | MODIFIER | c.-3546G>A| |
S199 |
| 132557 | BAA10g19430 | A10 | 17820405 | G | A | upstream_gene_variant | MODIFIER | c.-4850C>T| |
S162 |
| 132558 | BAA10g19430-BAA10g19440 | A10 | 17820725 | C | T | intergenic_region | MODIFIER | n.17820725C>T| |
S168 |
| 132559 | BAA10g19430-BAA10g19440 | A10 | 17821649 | C | T | intergenic_region | MODIFIER | n.17821649C>T| |
S37 |
| 132560 | BAA10g19440 | A10 | 17822886 | G | A | upstream_gene_variant | MODIFIER | c.-4328G>A| |
S240 |
| 132561 | BAA10g19440 | A10 | 17823416 | C | T | upstream_gene_variant | MODIFIER | c.-3798C>T| |
S153 S213 |
| 132562 | BAA10g19440 | A10 | 17823443 | C | T | upstream_gene_variant | MODIFIER | c.-3771C>T| |
S199 |
| 132563 | BAA10g19440 | A10 | 17823525 | G | A | upstream_gene_variant | MODIFIER | c.-3689G>A| |
S136 |
| 132564 | BAA10g19440 | A10 | 17823632 | G | A | upstream_gene_variant | MODIFIER | c.-3582G>A| |
S288 |
| 132565 | BAA10g19440 | A10 | 17823758 | G | A | upstream_gene_variant | MODIFIER | c.-3456G>A| |
S303 |
| 132566 | BAA10g19440 | A10 | 17823796 | G | A | upstream_gene_variant | MODIFIER | c.-3418G>A| |
S219 |
| 132567 | BAA10g19440 | A10 | 17824504 | G | A | upstream_gene_variant | MODIFIER | c.-2710G>A| |
S38 |
| 132568 | BAA10g19440 | A10 | 17825406 | C | T | upstream_gene_variant | MODIFIER | c.-1808C>T| |
S211 S227 |
| 132569 | BAA10g19440 | A10 | 17827152 | G | A | upstream_gene_variant | MODIFIER | c.-62G>A| |
S131 |
| 132570 | BAA10g19440 | A10 | 17827731 | C | T | missense_variant | MODERATE | c.518C>T|p.Ser173Phe |
S235 |
| 132571 | BAA10g19440 | A10 | 17828101 | G | A | downstream_gene_variant | MODIFIER | c.*75G>A| |
S69 |
| 132572 | BAA10g19440 | A10 | 17828327 | G | A | downstream_gene_variant | MODIFIER | c.*301G>A| |
S90 |
| 132573 | BAA10g19440 | A10 | 17828330 | G | A | downstream_gene_variant | MODIFIER | c.*304G>A| |
S288 |
| 132574 | BAA10g19460 | A10 | 17828659 | C | T | upstream_gene_variant | MODIFIER | c.-4956C>T| |
S212 |
| 132575 | BAA10g19450 | A10 | 17828978 | C | T | missense_variant | MODERATE | c.1195G>A|p.Asp399Asn |
S48 |