| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 113601 | BAA10g08950 | A10 | 10990345 | C | T | downstream_gene_variant | MODIFIER | c.*4664G>A| |
S114 |
| 113602 | BAA10g08950 | A10 | 10991312 | C | T | downstream_gene_variant | MODIFIER | c.*3697G>A| |
S281 |
| 113603 | BAA10g08950 | A10 | 10991605 | G | A | downstream_gene_variant | MODIFIER | c.*3404C>T| |
S55 |
| 113604 | BAA10g08950 | A10 | 10992117 | T | C | downstream_gene_variant | MODIFIER | c.*2892A>G| |
S240 |
| 113605 | BAA10g08950 | A10 | 10992237 | G | A | downstream_gene_variant | MODIFIER | c.*2772C>T| |
S129 |
| 113606 | BAA10g08950 | A10 | 10992254 | C | T | downstream_gene_variant | MODIFIER | c.*2755G>A| |
S144 S189 |
| 113607 | BAA10g08950 | A10 | 10992306 | G | A | downstream_gene_variant | MODIFIER | c.*2703C>T| |
S245 |
| 113608 | BAA10g08950 | A10 | 10995626 | G | A | intron_variant | MODIFIER | c.579+92C>T| |
S251 |
| 113609 | BAA10g08950 | A10 | 10996688 | C | T | intron_variant | MODIFIER | c.47-31G>A| |
S157 |
| 113610 | BAA10g08950 | A10 | 10996807 | C | T | stop_gained | HIGH | c.24G>A|p.Trp8* |
S42 |
| 113611 | BAA10g08950 | A10 | 10998491 | C | T | upstream_gene_variant | MODIFIER | c.-1661G>A| |
S173 |
| 113612 | BAA10g08950 | A10 | 10999897 | G | A | upstream_gene_variant | MODIFIER | c.-3067C>T| |
S15 S3 |
| 113613 | BAA10g08950 | A10 | 11000814 | C | T | upstream_gene_variant | MODIFIER | c.-3984G>A| |
S270 |
| 113614 | BAA10g08950 | A10 | 11000991 | C | T | upstream_gene_variant | MODIFIER | c.-4161G>A| |
S142 |
| 113615 | BAA10g08950 | A10 | 11001640 | G | A | upstream_gene_variant | MODIFIER | c.-4810C>T| |
S283 |
| 113616 | BAA10g08950-BAA10g08960 | A10 | 11002203 | C | T | intergenic_region | MODIFIER | n.11002203C>T| |
S124 |
| 113617 | BAA10g08950-BAA10g08960 | A10 | 11003621 | G | A | intergenic_region | MODIFIER | n.11003621G>A| |
S50 |
| 113618 | BAA10g08950-BAA10g08960 | A10 | 11004284 | G | A | intergenic_region | MODIFIER | n.11004284G>A| |
S238 |
| 113619 | BAA10g08950-BAA10g08960 | A10 | 11005388 | G | A | intergenic_region | MODIFIER | n.11005388G>A| |
S280 |
| 113620 | BAA10g08950-BAA10g08960 | A10 | 11005547 | C | T | intergenic_region | MODIFIER | n.11005547C>T| |
S131 |
| 113621 | BAA10g08960 | A10 | 11008627 | G | A | upstream_gene_variant | MODIFIER | c.-4867G>A| |
S303 |
| 113622 | BAA10g08960 | A10 | 11009148 | C | A | upstream_gene_variant | MODIFIER | c.-4346C>A| |
S8 |
| 113623 | BAA10g08960 | A10 | 11011820 | G | A | upstream_gene_variant | MODIFIER | c.-1674G>A| |
S70 |
| 113624 | BAA10g08960 | A10 | 11012527 | C | T | upstream_gene_variant | MODIFIER | c.-967C>T| |
S47 |
| 113625 | BAA10g08960 | A10 | 11013651 | C | T | missense_variant | MODERATE | c.158C>T|p.Ser53Leu |
S297 |