| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 140001 | BAA10g25170 | A10 | 20454087 | C | T | upstream_gene_variant | MODIFIER | c.-650C>T| |
S87 |
| 140002 | BAA10g25170 | A10 | 20454107 | C | T | upstream_gene_variant | MODIFIER | c.-630C>T| |
S25 |
| 140003 | BAA10g25190 | A10 | 20455908 | G | A | upstream_gene_variant | MODIFIER | c.-2170G>A| |
S190 |
| 140004 | BAA10g25190 | A10 | 20458604 | C | T | missense_variant | MODERATE | c.527C>T|p.Ser176Phe |
S298 |
| 140005 | BAA10g25190 | A10 | 20458649 | G | A | missense_variant | MODERATE | c.572G>A|p.Arg191Gln |
S197 |
| 140006 | BAA10g25190 | A10 | 20458970 | G | A | missense_variant | MODERATE | c.893G>A|p.Gly298Glu |
S219 S72 |
| 140007 | BAA10g25190 | A10 | 20459201 | C | T | missense_variant | MODERATE | c.1124C>T|p.Ala375Val |
S38 |
| 140008 | BAA10g25200 | A10 | 20460936 | C | T | missense_variant | MODERATE | c.514G>A|p.Gly172Arg |
S111 |
| 140009 | BAA10g25200 | A10 | 20461152 | C | T | missense_variant | MODERATE | c.394G>A|p.Glu132Lys |
S28 |
| 140010 | BAA10g25200 | A10 | 20463997 | G | A | upstream_gene_variant | MODIFIER | c.-2101C>T| |
S176 |
| 140011 | BAA10g25200 | A10 | 20464009 | G | A | upstream_gene_variant | MODIFIER | c.-2113C>T| |
S132 S137 S215 S237 |
| 140012 | BAA10g25200 | A10 | 20464286 | C | T | upstream_gene_variant | MODIFIER | c.-2390G>A| |
S161 |
| 140013 | BAA10g25200 | A10 | 20464828 | G | A | upstream_gene_variant | MODIFIER | c.-2932C>T| |
S82 S92 |
| 140014 | BAA10g25200 | A10 | 20465477 | G | A | upstream_gene_variant | MODIFIER | c.-3581C>T| |
S69 |
| 140015 | BAA10g25200 | A10 | 20465943 | G | A | upstream_gene_variant | MODIFIER | c.-4047C>T| |
S198 |
| 140016 | BAA10g25210 | A10 | 20465995 | C | T | synonymous_variant | LOW | c.42C>T|p.Phe14Phe |
S119 |
| 140017 | BAA10g25210 | A10 | 20466050 | C | T | missense_variant | MODERATE | c.97C>T|p.Leu33Phe |
S150 |
| 140018 | BAA10g25210 | A10 | 20467578 | G | A | missense_variant | MODERATE | c.640G>A|p.Val214Ile |
S136 |
| 140019 | BAA10g25210 | A10 | 20467628 | G | A | synonymous_variant | LOW | c.690G>A|p.Lys230Lys |
S207 |
| 140020 | BAA10g25210 | A10 | 20467636 | C | T | missense_variant | MODERATE | c.698C>T|p.Pro233Leu |
S155 S211 |
| 140021 | BAA10g25210 | A10 | 20467681 | C | T | missense_variant | MODERATE | c.743C>T|p.Pro248Leu |
S295 |
| 140022 | BAA10g25210 | A10 | 20467733 | C | T | synonymous_variant | LOW | c.795C>T|p.Leu265Leu |
S20 |
| 140023 | BAA10g25230 | A10 | 20468247 | G | A | upstream_gene_variant | MODIFIER | c.-3927G>A| |
S67 |
| 140024 | BAA10g25230 | A10 | 20468265 | G | A | upstream_gene_variant | MODIFIER | c.-3909G>A| |
S94 |
| 140025 | BAA10g25230 | A10 | 20468422 | C | T | upstream_gene_variant | MODIFIER | c.-3752C>T| |
S8 |