| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 78651 | BAA01g41370 | A01 | 27504053 | C | T | intron_variant | MODIFIER | c.1817-1080G>A| |
S104 S52 |
| 78652 | BAA01g41380 | A01 | 27504238 | C | T | upstream_gene_variant | MODIFIER | c.-4895C>T| |
S47 |
| 78653 | BAA01g41380 | A01 | 27504726 | C | T | upstream_gene_variant | MODIFIER | c.-4407C>T| |
S277 |
| 78654 | BAA01g41380 | A01 | 27504763 | G | A | upstream_gene_variant | MODIFIER | c.-4370G>A| |
S95 |
| 78655 | BAA01g41380 | A01 | 27505143 | C | T | upstream_gene_variant | MODIFIER | c.-3990C>T| |
S277 |
| 78656 | BAA01g41380 | A01 | 27505298 | C | T | upstream_gene_variant | MODIFIER | c.-3835C>T| |
S135 |
| 78657 | BAA01g41370 | A01 | 27505527 | C | T | missense_variant | MODERATE | c.1759G>A|p.Gly587Arg |
S192 |
| 78658 | BAA01g41370 | A01 | 27505692 | G | A | missense_variant | MODERATE | c.1679C>T|p.Thr560Ile |
S34 |
| 78659 | BAA01g41370 | A01 | 27506335 | C | T | missense_variant | MODERATE | c.1115G>A|p.Arg372Lys |
S64 |
| 78660 | BAA01g41370 | A01 | 27506493 | C | T | missense_variant | MODERATE | c.1031G>A|p.Gly344Asp |
S251 |
| 78661 | BAA01g41370 | A01 | 27506500 | C | T | missense_variant | MODERATE | c.1024G>A|p.Asp342Asn |
S103 |
| 78662 | BAA01g41370 | A01 | 27506536 | C | T | missense_variant | MODERATE | c.988G>A|p.Gly330Arg |
S69 |
| 78663 | BAA01g41370 | A01 | 27506674 | C | T | missense_variant | MODERATE | c.850G>A|p.Gly284Arg |
S1 S90 |
| 78664 | BAA01g41370 | A01 | 27506756 | C | T | splice_region_variant&intron_variant | LOW | c.838+5G>A| |
S242 |
| 78665 | BAA01g41370 | A01 | 27507278 | G | A | synonymous_variant | LOW | c.504C>T|p.Asn168Asn |
S293 |
| 78666 | BAA01g41370 | A01 | 27507750 | C | T | missense_variant | MODERATE | c.265G>A|p.Val89Ile |
S290 |
| 78667 | BAA01g41370 | A01 | 27508983 | C | T | upstream_gene_variant | MODIFIER | c.-969G>A| |
S274 |
| 78668 | BAA01g41370 | A01 | 27509130 | G | A | upstream_gene_variant | MODIFIER | c.-1116C>T| |
S158 |
| 78669 | BAA01g41380 | A01 | 27510496 | C | T | stop_gained | HIGH | c.535C>T|p.Arg179* |
S210 S225 |
| 78670 | BAA01g41370 | A01 | 27512343 | C | T | upstream_gene_variant | MODIFIER | c.-4329G>A| |
S183 |
| 78671 | BAA01g41370 | A01 | 27512958 | C | T | upstream_gene_variant | MODIFIER | c.-4944G>A| |
S183 |
| 78672 | BAA01g41380 | A01 | 27513311 | G | A | intron_variant | MODIFIER | c.1420-49G>A| |
S293 |
| 78673 | BAA01g41380 | A01 | 27513630 | G | A | missense_variant | MODERATE | c.1612G>A|p.Ala538Thr |
S144 |
| 78674 | BAA01g41380 | A01 | 27514152 | G | A | synonymous_variant | LOW | c.1698G>A|p.Pro566Pro |
S5 |
| 78675 | BAA01g41380 | A01 | 27515569 | G | A | missense_variant | MODERATE | c.2362G>A|p.Glu788Lys |
S208 |