| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 100251 | BAA10g06900 | A10 | 3692356 | G | A | upstream_gene_variant | MODIFIER | c.-971G>A| |
S252 |
| 100252 | BAA10g06890 | A10 | 3692511 | C | T | missense_variant | MODERATE | c.463G>A|p.Val155Ile |
S202 |
| 100253 | BAA10g06890 | A10 | 3692522 | G | A | missense_variant | MODERATE | c.452C>T|p.Pro151Leu |
S308 S66 |
| 100254 | BAA10g06890 | A10 | 3692549 | C | T | missense_variant | MODERATE | c.425G>A|p.Gly142Glu |
S203 |
| 100255 | BAA10g06890 | A10 | 3692784 | G | A | missense_variant | MODERATE | c.190C>T|p.Arg64Cys |
S112 |
| 100256 | BAA10g06890 | A10 | 3693052 | G | A | upstream_gene_variant | MODIFIER | c.-79C>T| |
S68 |
| 100257 | BAA10g06890 | A10 | 3693267 | C | T | upstream_gene_variant | MODIFIER | c.-294G>A| |
S23 |
| 100258 | BAA10g06890 | A10 | 3693277 | C | T | upstream_gene_variant | MODIFIER | c.-304G>A| |
S144 |
| 100259 | BAA10g06900 | A10 | 3694001 | C | T | synonymous_variant | LOW | c.675C>T|p.Leu225Leu |
S47 |
| 100260 | BAA10g06890 | A10 | 3694635 | C | T | upstream_gene_variant | MODIFIER | c.-1662G>A| |
S20 |
| 100261 | BAA10g06910 | A10 | 3695071 | C | T | missense_variant | MODERATE | c.2428G>A|p.Ala810Thr |
S95 |
| 100262 | BAA10g06910 | A10 | 3695403 | G | A | missense_variant | MODERATE | c.2096C>T|p.Pro699Leu |
S192 |
| 100263 | BAA10g06910 | A10 | 3695653 | C | T | missense_variant | MODERATE | c.1846G>A|p.Glu616Lys |
S195 |
| 100264 | BAA10g06910 | A10 | 3696261 | G | A | missense_variant | MODERATE | c.1646C>T|p.Ala549Val |
S39 |
| 100265 | BAA10g06910 | A10 | 3696464 | C | T | synonymous_variant | LOW | c.1443G>A|p.Lys481Lys |
S256 S259 |
| 100266 | BAA10g06910 | A10 | 3696556 | G | A | stop_gained | HIGH | c.1351C>T|p.Gln451* |
S13 |
| 100267 | BAA10g06910 | A10 | 3696935 | C | T | synonymous_variant | LOW | c.972G>A|p.Pro324Pro |
S14 S272 |
| 100268 | BAA10g06910 | A10 | 3697467 | C | T | missense_variant | MODERATE | c.551G>A|p.Gly184Glu |
S288 |
| 100269 | BAA10g06910 | A10 | 3697987 | G | A | missense_variant | MODERATE | c.31C>T|p.Leu11Phe |
S33 |
| 100270 | BAA10g06910 | A10 | 3698783 | C | T | upstream_gene_variant | MODIFIER | c.-766G>A| |
S139 S249 |
| 100271 | BAA10g06910 | A10 | 3699459 | G | A | upstream_gene_variant | MODIFIER | c.-1442C>T| |
S25 |
| 100272 | BAA10g06910 | A10 | 3699803 | G | A | upstream_gene_variant | MODIFIER | c.-1786C>T| |
S198 |
| 100273 | BAA10g06910 | A10 | 3699907 | C | T | upstream_gene_variant | MODIFIER | c.-1890G>A| |
S308 |
| 100274 | BAA10g06910 | A10 | 3700334 | G | A | upstream_gene_variant | MODIFIER | c.-2317C>T| |
S192 |
| 100275 | BAA10g06910 | A10 | 3700462 | C | T | upstream_gene_variant | MODIFIER | c.-2445G>A| |
S143 |