| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 79901 | BAA01g42060 | A01 | 27965614 | C | T | upstream_gene_variant | MODIFIER | c.-1282C>T| |
S94 |
| 79902 | BAA01g42060 | A01 | 27965833 | G | T | upstream_gene_variant | MODIFIER | c.-1063G>T| |
S242 |
| 79903 | BAA01g42070 | A01 | 27969324 | G | A | missense_variant | MODERATE | c.116C>T|p.Ser39Phe |
S181 |
| 79904 | BAA01g42070 | A01 | 27969761 | C | T | upstream_gene_variant | MODIFIER | c.-322G>A| |
S255 |
| 79905 | BAA01g42070 | A01 | 27970201 | C | T | upstream_gene_variant | MODIFIER | c.-762G>A| |
S236 |
| 79906 | BAA01g42080 | A01 | 27970617 | C | T | missense_variant | MODERATE | c.185C>T|p.Ser62Phe |
S127 |
| 79907 | BAA01g42080 | A01 | 27971108 | G | A | missense_variant | MODERATE | c.425G>A|p.Gly142Glu |
S187 |
| 79908 | BAA01g42080 | A01 | 27971143 | C | T | missense_variant | MODERATE | c.460C>T|p.Pro154Ser |
S15 S156 S3 S34 |
| 79909 | BAA01g42080 | A01 | 27971644 | G | A | synonymous_variant | LOW | c.879G>A|p.Ser293Ser |
S245 |
| 79910 | BAA01g42080 | A01 | 27971930 | C | T | missense_variant | MODERATE | c.1165C>T|p.Pro389Ser |
S56 |
| 79911 | BAA01g42080 | A01 | 27972182 | G | A | missense_variant | MODERATE | c.1417G>A|p.Val473Ile |
S142 |
| 79912 | BAA01g42090 | A01 | 27974390 | C | T | missense_variant | MODERATE | c.413G>A|p.Gly138Asp |
S241 |
| 79913 | BAA01g42090 | A01 | 27974711 | G | A | missense_variant | MODERATE | c.92C>T|p.Pro31Leu |
S191 |
| 79914 | BAA01g42090 | A01 | 27977958 | C | T | upstream_gene_variant | MODIFIER | c.-3156G>A| |
S134 |
| 79915 | BAA01g42100 | A01 | 27981002 | C | T | upstream_gene_variant | MODIFIER | c.-3602G>A| |
S247 |
| 79916 | BAA01g42100 | A01 | 27982267 | G | A | upstream_gene_variant | MODIFIER | c.-4867C>T| |
S278 |
| 79917 | BAA01g42120 | A01 | 27982499 | C | T | synonymous_variant | LOW | c.273C>T|p.Ile91Ile |
S57 |
| 79918 | BAA01g42120 | A01 | 27982588 | G | A | missense_variant | MODERATE | c.362G>A|p.Gly121Glu |
S139 |
| 79919 | BAA01g42120 | A01 | 27982722 | A | T | missense_variant | MODERATE | c.496A>T|p.Ile166Phe |
S232 |
| 79920 | BAA01g42120 | A01 | 27983203 | G | A | missense_variant | MODERATE | c.895G>A|p.Ala299Thr |
S286 |
| 79921 | BAA01g42110 | A01 | 27983898 | G | A | upstream_gene_variant | MODIFIER | c.-3189C>T| |
S79 S91 |
| 79922 | BAA01g42130 | A01 | 27985730 | G | A | missense_variant | MODERATE | c.178C>T|p.Pro60Ser |
S172 S217 |
| 79923 | BAA01g42130 | A01 | 27986003 | C | T | upstream_gene_variant | MODIFIER | c.-96G>A| |
S118 |
| 79924 | BAA01g42130 | A01 | 27986042 | C | T | upstream_gene_variant | MODIFIER | c.-135G>A| |
S115 |
| 79925 | BAA01g42130 | A01 | 27988225 | G | A | upstream_gene_variant | MODIFIER | c.-2318C>T| |
S294 |