| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 83851 | BAA01g44460 | A01 | 29546759 | C | T | upstream_gene_variant | MODIFIER | c.-1195C>T| |
S155 |
| 83852 | BAA01g44460 | A01 | 29549655 | C | T | missense_variant | MODERATE | c.1001C>T|p.Pro334Leu |
S32 |
| 83853 | BAA01g44450 | A01 | 29549704 | G | A | downstream_gene_variant | MODIFIER | c.*4964G>A| |
S83 S88 |
| 83854 | BAA01g44460 | A01 | 29551766 | C | T | downstream_gene_variant | MODIFIER | c.*417C>T| |
S240 |
| 83855 | BAA01g44460 | A01 | 29551790 | G | A | downstream_gene_variant | MODIFIER | c.*441G>A| |
S274 |
| 83856 | BAA01g44480 | A01 | 29552579 | C | T | upstream_gene_variant | MODIFIER | c.-4588C>T| |
S205 |
| 83857 | BAA01g44480 | A01 | 29553650 | C | T | upstream_gene_variant | MODIFIER | c.-3517C>T| |
S19 |
| 83858 | BAA01g44480 | A01 | 29553781 | G | A | upstream_gene_variant | MODIFIER | c.-3386G>A| |
S176 |
| 83859 | BAA01g44480 | A01 | 29553957 | C | T | upstream_gene_variant | MODIFIER | c.-3210C>T| |
S242 |
| 83860 | BAA01g44470 | A01 | 29555459 | G | A | missense_variant | MODERATE | c.304C>T|p.Pro102Ser |
S208 S219 |
| 83861 | BAA01g44470 | A01 | 29556427 | T | A | upstream_gene_variant | MODIFIER | c.-665A>T| |
S160 |
| 83862 | BAA01g44470 | A01 | 29556483 | C | T | upstream_gene_variant | MODIFIER | c.-721G>A| |
S107 |
| 83863 | BAA01g44470 | A01 | 29556892 | G | A | upstream_gene_variant | MODIFIER | c.-1130C>T| |
S159 S188 S202 S298 |
| 83864 | BAA01g44480 | A01 | 29558074 | G | A | splice_donor_variant&intron_variant | HIGH | c.437+1G>A| |
S223 |
| 83865 | BAA01g44480 | A01 | 29558665 | C | T | synonymous_variant | LOW | c.615C>T|p.His205His |
S159 |
| 83866 | BAA01g44480 | A01 | 29559104 | C | T | synonymous_variant | LOW | c.975C>T|p.Ser325Ser |
S183 S198 |
| 83867 | BAA01g44480 | A01 | 29559135 | G | A | missense_variant | MODERATE | c.1006G>A|p.Ala336Thr |
S217 S248 |
| 83868 | BAA01g44470 | A01 | 29559517 | C | T | upstream_gene_variant | MODIFIER | c.-3755G>A| |
S111 |
| 83869 | BAA01g44480 | A01 | 29560116 | C | T | stop_gained | HIGH | c.1426C>T|p.Arg476* |
S216 |
| 83870 | BAA01g44480 | A01 | 29561606 | C | T | downstream_gene_variant | MODIFIER | c.*834C>T| |
S78 S83 |
| 83871 | BAA01g44480 | A01 | 29561620 | C | T | downstream_gene_variant | MODIFIER | c.*848C>T| |
S286 |
| 83872 | BAA01g44480 | A01 | 29561877 | G | A | downstream_gene_variant | MODIFIER | c.*1105G>A| |
S87 |
| 83873 | BAA01g44480 | A01 | 29561930 | C | T | downstream_gene_variant | MODIFIER | c.*1158C>T| |
S182 |
| 83874 | BAA01g44480 | A01 | 29562650 | G | T | downstream_gene_variant | MODIFIER | c.*1878G>T| |
S166 |
| 83875 | BAA01g44480 | A01 | 29562907 | C | T | downstream_gene_variant | MODIFIER | c.*2135C>T| |
S233 |