| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 139551 | BAA10g24750 | A10 | 20290209 | C | T | upstream_gene_variant | MODIFIER | c.-2481G>A| |
S34 |
| 139552 | BAA10g24760 | A10 | 20290309 | C | T | missense_variant | MODERATE | c.596C>T|p.Ser199Phe |
S183 |
| 139553 | BAA10g24750 | A10 | 20290672 | G | A | upstream_gene_variant | MODIFIER | c.-2944C>T| |
S179 |
| 139554 | BAA10g24750 | A10 | 20291770 | C | T | upstream_gene_variant | MODIFIER | c.-4042G>A| |
S47 |
| 139555 | BAA10g24790 | A10 | 20293101 | C | T | upstream_gene_variant | MODIFIER | c.-3830C>T| |
S177 |
| 139556 | BAA10g24790 | A10 | 20293540 | C | T | upstream_gene_variant | MODIFIER | c.-3391C>T| |
S247 |
| 139557 | BAA10g24770 | A10 | 20293818 | C | T | missense_variant | MODERATE | c.761C>T|p.Ser254Phe |
S79 S91 |
| 139558 | BAA10g24790 | A10 | 20294563 | G | A | upstream_gene_variant | MODIFIER | c.-2368G>A| |
S163 |
| 139559 | BAA10g24780 | A10 | 20294602 | G | A | missense_variant | MODERATE | c.343C>T|p.Leu115Phe |
S75 S81 |
| 139560 | BAA10g24780 | A10 | 20296060 | G | A | upstream_gene_variant | MODIFIER | c.-1048C>T| |
S264 |
| 139561 | BAA10g24790 | A10 | 20297863 | G | A | missense_variant | MODERATE | c.634G>A|p.Ala212Thr |
S83 S88 |
| 139562 | BAA10g24780 | A10 | 20298470 | C | T | upstream_gene_variant | MODIFIER | c.-3458G>A| |
S275 |
| 139563 | BAA10g24780 | A10 | 20299519 | C | T | upstream_gene_variant | MODIFIER | c.-4507G>A| |
S25 |
| 139564 | BAA10g24780 | A10 | 20299755 | C | T | upstream_gene_variant | MODIFIER | c.-4743G>A| |
S259 |
| 139565 | BAA10g24790 | A10 | 20300258 | C | T | downstream_gene_variant | MODIFIER | c.*2120C>T| |
S262 |
| 139566 | BAA10g24800 | A10 | 20300626 | G | A | stop_gained | HIGH | c.1423C>T|p.Gln475* |
S241 |
| 139567 | BAA10g24790 | A10 | 20301582 | G | A | downstream_gene_variant | MODIFIER | c.*3444G>A| |
S223 |
| 139568 | BAA10g24790 | A10 | 20301784 | G | A | downstream_gene_variant | MODIFIER | c.*3646G>A| |
S250 |
| 139569 | BAA10g24790 | A10 | 20301797 | G | A | downstream_gene_variant | MODIFIER | c.*3659G>A| |
S219 |
| 139570 | BAA10g24800 | A10 | 20302159 | G | A | synonymous_variant | LOW | c.438C>T|p.Leu146Leu |
S166 S37 |
| 139571 | BAA10g24800 | A10 | 20302989 | C | T | upstream_gene_variant | MODIFIER | c.-216G>A| |
S146 |
| 139572 | BAA10g24810 | A10 | 20303715 | G | A | missense_variant | MODERATE | c.2096C>T|p.Pro699Leu |
S53 |
| 139573 | BAA10g24810 | A10 | 20304217 | C | T | missense_variant | MODERATE | c.1801G>A|p.Glu601Lys |
S78 |
| 139574 | BAA10g24800 | A10 | 20305126 | G | A | upstream_gene_variant | MODIFIER | c.-2353C>T| |
S16 |
| 139575 | BAA10g24810 | A10 | 20305517 | C | T | missense_variant | MODERATE | c.1133G>A|p.Gly378Glu |
S168 |