| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 147851 | BAA10g32260 | A10 | 23249473 | G | A | upstream_gene_variant | MODIFIER | c.-3979C>T| |
S140 S168 S278 S64 |
| 147852 | BAA10g32260 | A10 | 23249763 | G | A | upstream_gene_variant | MODIFIER | c.-4269C>T| |
S181 |
| 147853 | BAA10g32270 | A10 | 23250059 | C | T | missense_variant | MODERATE | c.197C>T|p.Ser66Phe |
S66 |
| 147854 | BAA10g32280 | A10 | 23253892 | G | A | upstream_gene_variant | MODIFIER | c.-2673G>A| |
S159 S243 |
| 147855 | BAA10g32280 | A10 | 23254251 | G | A | upstream_gene_variant | MODIFIER | c.-2314G>A| |
S240 |
| 147856 | BAA10g32280 | A10 | 23254790 | G | A | upstream_gene_variant | MODIFIER | c.-1775G>A| |
S183 S198 |
| 147857 | BAA10g32280 | A10 | 23256191 | C | T | upstream_gene_variant | MODIFIER | c.-374C>T| |
S177 |
| 147858 | BAA10g32290 | A10 | 23256633 | G | A | downstream_gene_variant | MODIFIER | c.*2272C>T| |
S179 |
| 147859 | BAA10g32290 | A10 | 23256708 | C | T | downstream_gene_variant | MODIFIER | c.*2197G>A| |
S119 |
| 147860 | BAA10g32280 | A10 | 23257452 | G | A | downstream_gene_variant | MODIFIER | c.*381G>A| |
S280 |
| 147861 | BAA10g32280 | A10 | 23258552 | G | A | downstream_gene_variant | MODIFIER | c.*1481G>A| |
S131 |
| 147862 | BAA10g32280 | A10 | 23259236 | G | A | downstream_gene_variant | MODIFIER | c.*2165G>A| |
S265 |
| 147863 | BAA10g32280 | A10 | 23259524 | G | A | downstream_gene_variant | MODIFIER | c.*2453G>A| |
S263 |
| 147864 | BAA10g32290 | A10 | 23260201 | C | T | upstream_gene_variant | MODIFIER | c.-492G>A| |
S2 |
| 147865 | BAA10g32290 | A10 | 23264507 | C | T | upstream_gene_variant | MODIFIER | c.-4798G>A| |
S177 |
| 147866 | BAA10g32300 | A10 | 23264902 | C | T | downstream_gene_variant | MODIFIER | c.*674G>A| |
S19 |
| 147867 | BAA10g32300 | A10 | 23265698 | G | A | missense_variant | MODERATE | c.1309C>T|p.Pro437Ser |
S183 S198 |
| 147868 | BAA10g32300 | A10 | 23265871 | C | T | missense_variant | MODERATE | c.1136G>A|p.Arg379Lys |
S129 |
| 147869 | BAA10g32300 | A10 | 23266484 | C | T | intron_variant | MODIFIER | c.859-249G>A| |
S114 |
| 147870 | BAA10g32310 | A10 | 23266683 | C | T | upstream_gene_variant | MODIFIER | c.-4830C>T| |
S140 |
| 147871 | BAA10g32310 | A10 | 23266725 | G | A | upstream_gene_variant | MODIFIER | c.-4788G>A| |
S199 |
| 147872 | BAA10g32300 | A10 | 23267044 | C | T | missense_variant | MODERATE | c.820G>A|p.Asp274Asn |
S45 |
| 147873 | BAA10g32300 | A10 | 23267810 | G | A | stop_gained | HIGH | c.265C>T|p.Gln89* |
S270 |
| 147874 | BAA10g32300 | A10 | 23270079 | A | G | upstream_gene_variant | MODIFIER | c.-123T>C| |
S139 |
| 147875 | BAA10g32300 | A10 | 23270299 | C | A | upstream_gene_variant | MODIFIER | c.-343G>T| |
S182 |