| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 150551 | BAA10g34520 | A10 | 24247997 | G | A | upstream_gene_variant | MODIFIER | c.-1247G>A| |
S131 |
| 150552 | BAA10g34510 | A10 | 24248358 | G | A | missense_variant | MODERATE | c.221C>T|p.Ser74Phe |
S240 |
| 150553 | BAA10g34530 | A10 | 24252549 | G | A | synonymous_variant | LOW | c.726C>T|p.Pro242Pro |
S280 |
| 150554 | BAA10g34530 | A10 | 24252586 | G | A | missense_variant | MODERATE | c.689C>T|p.Ser230Phe |
S127 |
| 150555 | BAA10g34530 | A10 | 24252642 | G | A | synonymous_variant | LOW | c.633C>T|p.Asn211Asn |
S284 |
| 150556 | BAA10g34510 | A10 | 24253460 | A | G | upstream_gene_variant | MODIFIER | c.-4561T>C| |
S183 S198 |
| 150557 | BAA10g34530 | A10 | 24253939 | G | A | synonymous_variant | LOW | c.330C>T|p.Phe110Phe |
S99 |
| 150558 | BAA10g34530 | A10 | 24253974 | C | T | missense_variant | MODERATE | c.295G>A|p.Gly99Arg |
S23 |
| 150559 | BAA10g34530 | A10 | 24254227 | G | A | missense_variant | MODERATE | c.128C>T|p.Ala43Val |
S185 |
| 150560 | BAA10g34530 | A10 | 24254442 | G | A | upstream_gene_variant | MODIFIER | c.-88C>T| |
S233 |
| 150561 | BAA10g34530 | A10 | 24254840 | C | T | upstream_gene_variant | MODIFIER | c.-486G>A| |
S18 |
| 150562 | BAA10g34530 | A10 | 24255995 | G | A | upstream_gene_variant | MODIFIER | c.-1641C>T| |
S62 |
| 150563 | BAA10g34530 | A10 | 24256770 | C | T | upstream_gene_variant | MODIFIER | c.-2416G>A| |
S110 |
| 150564 | BAA10g34540 | A10 | 24257208 | C | T | splice_region_variant&stop_retained_variant | LOW | c.2403G>A|p.Ter801Ter |
S121 |
| 150565 | BAA10g34540 | A10 | 24257299 | G | A | missense_variant | MODERATE | c.2312C>T|p.Ser771Leu |
S189 |
| 150566 | BAA10g34540 | A10 | 24257906 | G | A | missense_variant | MODERATE | c.1939C>T|p.Arg647Cys |
S290 |
| 150567 | BAA10g34540 | A10 | 24258756 | G | A | splice_region_variant&intron_variant | LOW | c.1350-4C>T| |
S57 |
| 150568 | BAA10g34540 | A10 | 24260312 | C | T | missense_variant | MODERATE | c.653G>A|p.Gly218Asp |
S287 |
| 150569 | BAA10g34540 | A10 | 24260394 | G | A | missense_variant | MODERATE | c.638C>T|p.Ala213Val |
S32 |
| 150570 | BAA10g34540 | A10 | 24260676 | G | A | stop_gained | HIGH | c.478C>T|p.Gln160* |
S290 |
| 150571 | BAA10g34550 | A10 | 24260738 | C | T | downstream_gene_variant | MODIFIER | c.*897G>A| |
S176 |
| 150572 | BAA10g34540 | A10 | 24261540 | G | A | upstream_gene_variant | MODIFIER | c.-248C>T| |
S125 |
| 150573 | BAA10g34550 | A10 | 24261643 | G | A | missense_variant | MODERATE | c.754C>T|p.Arg252Cys |
S233 |
| 150574 | BAA10g34550 | A10 | 24262458 | C | T | stop_gained | HIGH | c.330G>A|p.Trp110* |
S232 |
| 150575 | BAA10g34550 | A10 | 24262632 | C | T | missense_variant | MODERATE | c.233G>A|p.Ser78Asn |
S36 |