| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 12401 | BAA01g09860 | A01 | 4423219 | C | T | upstream_gene_variant | MODIFIER | c.-2658G>A| |
S70 |
| 12402 | BAA01g09860 | A01 | 4423220 | C | T | upstream_gene_variant | MODIFIER | c.-2659G>A| |
S39 |
| 12403 | BAA01g09870 | A01 | 4423570 | C | T | missense_variant | MODERATE | c.2695G>A|p.Glu899Lys |
S25 |
| 12404 | BAA01g09870 | A01 | 4424360 | C | T | missense_variant | MODERATE | c.1990G>A|p.Ala664Thr |
S135 |
| 12405 | BAA01g09870 | A01 | 4424633 | C | T | missense_variant | MODERATE | c.1717G>A|p.Val573Ile |
S295 |
| 12406 | BAA01g09870 | A01 | 4424795 | G | A | missense_variant | MODERATE | c.1555C>T|p.Arg519Cys |
S281 |
| 12407 | BAA01g09870 | A01 | 4424811 | C | T | synonymous_variant | LOW | c.1539G>A|p.Glu513Glu |
S169 |
| 12408 | BAA01g09870 | A01 | 4426447 | G | A | upstream_gene_variant | MODIFIER | c.-98C>T| |
S296 |
| 12409 | BAA01g09870 | A01 | 4426653 | G | A | upstream_gene_variant | MODIFIER | c.-304C>T| |
S293 |
| 12410 | BAA01g09870 | A01 | 4427421 | G | A | upstream_gene_variant | MODIFIER | c.-1072C>T| |
S10 |
| 12411 | BAA01g09880 | A01 | 4428421 | C | T | missense_variant | MODERATE | c.56C>T|p.Pro19Leu |
S284 |
| 12412 | BAA01g09890 | A01 | 4429610 | C | T | synonymous_variant | LOW | c.645G>A|p.Glu215Glu |
S40 S49 |
| 12413 | BAA01g09870 | A01 | 4430547 | C | T | upstream_gene_variant | MODIFIER | c.-4198G>A| |
S179 |
| 12414 | BAA01g09890 | A01 | 4430705 | C | T | synonymous_variant | LOW | c.144G>A|p.Lys48Lys |
S277 |
| 12415 | BAA01g09870 | A01 | 4430862 | C | T | upstream_gene_variant | MODIFIER | c.-4513G>A| |
S282 |
| 12416 | BAA01g09870 | A01 | 4431224 | G | A | upstream_gene_variant | MODIFIER | c.-4875C>T| |
S202 |
| 12417 | BAA01g09900 | A01 | 4431721 | G | A | synonymous_variant | LOW | c.165G>A|p.Glu55Glu |
S241 |
| 12418 | BAA01g09900 | A01 | 4432060 | C | T | splice_region_variant&intron_variant | LOW | c.339+7C>T| |
S218 |
| 12419 | BAA01g09900 | A01 | 4433049 | G | A | missense_variant | MODERATE | c.674G>A|p.Cys225Tyr |
S10 |
| 12420 | BAA01g09900 | A01 | 4433591 | G | A | missense_variant&splice_region_variant | MODERATE | c.890G>A|p.Gly297Asp |
S131 |
| 12421 | BAA01g09900 | A01 | 4433602 | G | A | missense_variant | MODERATE | c.901G>A|p.Glu301Lys |
S239 |
| 12422 | BAA01g09890 | A01 | 4434006 | C | T | upstream_gene_variant | MODIFIER | c.-3158G>A| |
S184 |
| 12423 | BAA01g09900 | A01 | 4434505 | G | A | missense_variant | MODERATE | c.1454G>A|p.Gly485Asp |
S139 |
| 12424 | BAA01g09900 | A01 | 4434974 | C | T | missense_variant | MODERATE | c.1745C>T|p.Ala582Val |
S171 |
| 12425 | BAA01g09900 | A01 | 4435645 | C | T | synonymous_variant | LOW | c.2175C>T|p.Gly725Gly |
S200 |