| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 21201 | BAA01g15460 | A01 | 7467128 | C | T | upstream_gene_variant | MODIFIER | c.-1948C>T| |
S291 |
| 21202 | BAA01g15460 | A01 | 7468712 | C | T | upstream_gene_variant | MODIFIER | c.-364C>T| |
S65 |
| 21203 | BAA01g15460 | A01 | 7469060 | G | A | upstream_gene_variant | MODIFIER | c.-16G>A| |
S23 |
| 21204 | BAA01g15460 | A01 | 7470262 | G | A | synonymous_variant | LOW | c.777G>A|p.Ala259Ala |
S163 |
| 21205 | BAA01g15460 | A01 | 7470481 | C | T | missense_variant | MODERATE | c.859C>T|p.Pro287Ser |
S305 |
| 21206 | BAA01g15460 | A01 | 7470704 | C | T | synonymous_variant | LOW | c.972C>T|p.Val324Val |
S289 S290 |
| 21207 | BAA01g15470 | A01 | 7472468 | G | A | upstream_gene_variant | MODIFIER | c.-4567G>A| |
S34 |
| 21208 | BAA01g15470 | A01 | 7472915 | G | A | upstream_gene_variant | MODIFIER | c.-4120G>A| |
S174 |
| 21209 | BAA01g15470 | A01 | 7472964 | G | A | upstream_gene_variant | MODIFIER | c.-4071G>A| |
S138 |
| 21210 | BAA01g15470 | A01 | 7473204 | C | T | upstream_gene_variant | MODIFIER | c.-3831C>T| |
S53 |
| 21211 | BAA01g15470 | A01 | 7474560 | C | T | upstream_gene_variant | MODIFIER | c.-2475C>T| |
S10 |
| 21212 | BAA01g15470 | A01 | 7475124 | C | T | upstream_gene_variant | MODIFIER | c.-1911C>T| |
S62 |
| 21213 | BAA01g15470 | A01 | 7475427 | C | T | upstream_gene_variant | MODIFIER | c.-1608C>T| |
S182 |
| 21214 | BAA01g15470 | A01 | 7475534 | G | A | upstream_gene_variant | MODIFIER | c.-1501G>A| |
S178 |
| 21215 | BAA01g15470 | A01 | 7475793 | C | T | upstream_gene_variant | MODIFIER | c.-1242C>T| |
S226 |
| 21216 | BAA01g15470 | A01 | 7476157 | G | A | upstream_gene_variant | MODIFIER | c.-878G>A| |
S95 |
| 21217 | BAA01g15470 | A01 | 7477037 | G | A | start_lost | HIGH | c.3G>A|p.Met1? |
S243 |
| 21218 | BAA01g15490 | A01 | 7478477 | C | T | upstream_gene_variant | MODIFIER | c.-2592C>T| |
S230 |
| 21219 | BAA01g15480 | A01 | 7478931 | G | A | splice_region_variant&intron_variant | LOW | c.417+8C>T| |
S263 |
| 21220 | BAA01g15480 | A01 | 7478991 | G | A | missense_variant | MODERATE | c.365C>T|p.Ser122Phe |
S186 |
| 21221 | BAA01g15480 | A01 | 7479631 | C | T | upstream_gene_variant | MODIFIER | c.-276G>A| |
S44 |
| 21222 | BAA01g15480 | A01 | 7480192 | C | T | upstream_gene_variant | MODIFIER | c.-837G>A| |
S305 |
| 21223 | BAA01g15480 | A01 | 7480974 | G | A | upstream_gene_variant | MODIFIER | c.-1619C>T| |
S211 |
| 21224 | BAA01g15490 | A01 | 7481252 | G | A | missense_variant | MODERATE | c.184G>A|p.Glu62Lys |
S129 |
| 21225 | BAA01g15490 | A01 | 7482266 | C | T | missense_variant | MODERATE | c.805C>T|p.Pro269Ser |
S231 |