| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 48001 | BAA01g27670 | A01 | 16657584 | C | T | downstream_gene_variant | MODIFIER | c.*3966C>T| |
S284 |
| 48002 | BAA01g27670 | A01 | 16658400 | C | T | downstream_gene_variant | MODIFIER | c.*4782C>T| |
S19 |
| 48003 | BAA01g27670 | A01 | 16658511 | G | A | downstream_gene_variant | MODIFIER | c.*4893G>A| |
S187 |
| 48004 | BAA01g27690 | A01 | 16662792 | G | A | upstream_gene_variant | MODIFIER | c.-1291G>A| |
S241 |
| 48005 | BAA01g27680 | A01 | 16663654 | G | A | upstream_gene_variant | MODIFIER | c.-494C>T| |
|
| 48006 | BAA01g27680 | A01 | 16663941 | C | T | upstream_gene_variant | MODIFIER | c.-781G>A| |
S152 |
| 48007 | BAA01g27690 | A01 | 16664278 | C | T | missense_variant | MODERATE | c.196C>T|p.Pro66Ser |
S136 |
| 48008 | BAA01g27700 | A01 | 16665177 | G | A | missense_variant | MODERATE | c.1480C>T|p.Pro494Ser |
S140 |
| 48009 | BAA01g27700 | A01 | 16665974 | C | T | missense_variant | MODERATE | c.1013G>A|p.Gly338Glu |
S153 |
| 48010 | BAA01g27700 | A01 | 16666785 | C | T | missense_variant | MODERATE | c.667G>A|p.Ala223Thr |
S42 |
| 48011 | BAA01g27680 | A01 | 16667735 | C | T | upstream_gene_variant | MODIFIER | c.-4575G>A| |
S205 |
| 48012 | BAA01g27680 | A01 | 16668104 | G | A | upstream_gene_variant | MODIFIER | c.-4944C>T| |
S284 |
| 48013 | BAA01g27710 | A01 | 16669602 | C | T | downstream_gene_variant | MODIFIER | c.*2025G>A| |
S289 S290 |
| 48014 | BAA01g27710 | A01 | 16669621 | G | C | downstream_gene_variant | MODIFIER | c.*2006C>G| |
S35 |
| 48015 | BAA01g27700 | A01 | 16670079 | C | T | synonymous_variant | LOW | c.123G>A|p.Leu41Leu |
S237 |
| 48016 | BAA01g27700 | A01 | 16670307 | G | A | upstream_gene_variant | MODIFIER | c.-106C>T| |
S74 |
| 48017 | BAA01g27700 | A01 | 16670764 | C | T | upstream_gene_variant | MODIFIER | c.-563G>A| |
S131 |
| 48018 | BAA01g27700 | A01 | 16670829 | C | T | upstream_gene_variant | MODIFIER | c.-628G>A| |
S134 |
| 48019 | BAA01g27700 | A01 | 16670841 | G | A | upstream_gene_variant | MODIFIER | c.-640C>T| |
S70 |
| 48020 | BAA01g27710 | A01 | 16671654 | C | T | synonymous_variant | LOW | c.327G>A|p.Lys109Lys |
S47 |
| 48021 | BAA01g27720 | A01 | 16673426 | G | A | missense_variant | MODERATE | c.1097C>T|p.Ser366Phe |
S306 S308 |
| 48022 | BAA01g27720 | A01 | 16673795 | G | A | missense_variant | MODERATE | c.911C>T|p.Ala304Val |
S163 |
| 48023 | BAA01g27720 | A01 | 16673829 | C | T | missense_variant | MODERATE | c.877G>A|p.Asp293Asn |
S112 |
| 48024 | BAA01g27720 | A01 | 16673863 | C | T | synonymous_variant | LOW | c.843G>A|p.Lys281Lys |
S46 |
| 48025 | BAA01g27720 | A01 | 16674049 | G | A | missense_variant | MODERATE | c.743C>T|p.Thr248Ile |
S169 |