| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 33851 | BAA01g22940 | A01 | 11682252 | G | A | downstream_gene_variant | MODIFIER | c.*3141G>A| |
S251 |
| 33852 | BAA01g22940 | A01 | 11682791 | T | A | downstream_gene_variant | MODIFIER | c.*3680T>A| |
S74 |
| 33853 | BAA01g22940 | A01 | 11682810 | C | T | downstream_gene_variant | MODIFIER | c.*3699C>T| |
S270 |
| 33854 | BAA01g22940 | A01 | 11683089 | G | A | downstream_gene_variant | MODIFIER | c.*3978G>A| |
S298 |
| 33855 | BAA01g22950 | A01 | 11683731 | C | T | missense_variant | MODERATE | c.641G>A|p.Gly214Glu |
S18 |
| 33856 | BAA01g22950 | A01 | 11686140 | G | A | upstream_gene_variant | MODIFIER | c.-1244C>T| |
S280 |
| 33857 | BAA01g22950 | A01 | 11686603 | C | T | upstream_gene_variant | MODIFIER | c.-1707G>A| |
S67 |
| 33858 | BAA01g22950 | A01 | 11686829 | C | T | upstream_gene_variant | MODIFIER | c.-1933G>A| |
S62 |
| 33859 | BAA01g22950 | A01 | 11687109 | C | T | upstream_gene_variant | MODIFIER | c.-2213G>A| |
S192 |
| 33860 | BAA01g22950 | A01 | 11687488 | G | A | upstream_gene_variant | MODIFIER | c.-2592C>T| |
S28 |
| 33861 | BAA01g22950 | A01 | 11688409 | A | T | upstream_gene_variant | MODIFIER | c.-3513T>A| |
S237 |
| 33862 | BAA01g22950 | A01 | 11688636 | C | T | upstream_gene_variant | MODIFIER | c.-3740G>A| |
S113 |
| 33863 | BAA01g22950 | A01 | 11689144 | G | A | upstream_gene_variant | MODIFIER | c.-4248C>T| |
S159 S243 |
| 33864 | BAA01g22950 | A01 | 11689394 | C | T | upstream_gene_variant | MODIFIER | c.-4498G>A| |
S294 |
| 33865 | BAA01g22960 | A01 | 11690085 | C | T | upstream_gene_variant | MODIFIER | c.-899C>T| |
S198 |
| 33866 | BAA01g22960 | A01 | 11692739 | C | T | missense_variant | MODERATE | c.451C>T|p.Leu151Phe |
S133 |
| 33867 | BAA01g22960 | A01 | 11693046 | C | T | missense_variant | MODERATE | c.758C>T|p.Ala253Val |
S47 |
| 33868 | BAA01g22960 | A01 | 11693186 | G | A | missense_variant | MODERATE | c.842G>A|p.Gly281Asp |
S199 |
| 33869 | BAA01g22960 | A01 | 11693199 | C | T | synonymous_variant | LOW | c.855C>T|p.Asn285Asn |
S130 |
| 33870 | BAA01g22960 | A01 | 11693282 | G | A | downstream_gene_variant | MODIFIER | c.*65G>A| |
S299 |
| 33871 | BAA01g22960 | A01 | 11695988 | G | A | downstream_gene_variant | MODIFIER | c.*2771G>A| |
S193 |
| 33872 | BAA01g22960 | A01 | 11696033 | G | A | downstream_gene_variant | MODIFIER | c.*2816G>A| |
S129 |
| 33873 | BAA01g22960 | A01 | 11697632 | G | A | downstream_gene_variant | MODIFIER | c.*4415G>A| |
S97 |
| 33874 | BAA01g22960 | A01 | 11697671 | G | A | downstream_gene_variant | MODIFIER | c.*4454G>A| |
S238 |
| 33875 | BAA01g22960 | A01 | 11697825 | G | A | downstream_gene_variant | MODIFIER | c.*4608G>A| |
S255 |