| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 174001 | BAA02g17010 | A02 | 8461465 | C | T | intron_variant | MODIFIER | c.1216-1768C>T| |
S265 |
| 174002 | BAA02g17010 | A02 | 8461930 | G | A | intron_variant | MODIFIER | c.1216-1303G>A| |
S229 |
| 174003 | BAA02g17010 | A02 | 8462646 | C | T | intron_variant | MODIFIER | c.1216-587C>T| |
S293 |
| 174004 | BAA02g17010 | A02 | 8462747 | G | A | intron_variant | MODIFIER | c.1216-486G>A| |
S132 S137 S215 S89 |
| 174005 | BAA02g17010 | A02 | 8463306 | C | T | missense_variant | MODERATE | c.1289C>T|p.Ser430Leu |
S262 |
| 174006 | BAA02g17010 | A02 | 8463586 | G | A | synonymous_variant | LOW | c.1485G>A|p.Pro495Pro |
S251 |
| 174007 | BAA02g17010 | A02 | 8463749 | G | A | missense_variant | MODERATE | c.1648G>A|p.Asp550Asn |
S206 S26 |
| 174008 | BAA02g17010 | A02 | 8464161 | C | T | missense_variant | MODERATE | c.2060C>T|p.Ser687Phe |
S139 |
| 174009 | BAA02g17010 | A02 | 8465566 | C | T | synonymous_variant | LOW | c.2994C>T|p.Leu998Leu |
S81 S85 |
| 174010 | BAA02g17010 | A02 | 8465573 | C | T | missense_variant | MODERATE | c.3001C>T|p.Pro1001Ser |
S244 |
| 174011 | BAA02g17010 | A02 | 8466936 | C | T | downstream_gene_variant | MODIFIER | c.*1331C>T| |
S163 |
| 174012 | BAA02g17010 | A02 | 8467191 | G | A | downstream_gene_variant | MODIFIER | c.*1586G>A| |
S34 |
| 174013 | BAA02g17010 | A02 | 8467825 | G | A | downstream_gene_variant | MODIFIER | c.*2220G>A| |
S148 S30 S31 |
| 174014 | BAA02g17010 | A02 | 8469036 | C | T | downstream_gene_variant | MODIFIER | c.*3431C>T| |
S60 |
| 174015 | BAA02g17030 | A02 | 8470046 | C | T | missense_variant | MODERATE | c.230G>A|p.Arg77Lys |
S5 |
| 174016 | BAA02g17020 | A02 | 8470852 | G | A | upstream_gene_variant | MODIFIER | c.-1434C>T| |
S20 |
| 174017 | BAA02g17020 | A02 | 8472167 | G | A | upstream_gene_variant | MODIFIER | c.-2749C>T| |
S125 |
| 174018 | BAA02g17020 | A02 | 8472366 | C | T | upstream_gene_variant | MODIFIER | c.-2948G>A| |
S165 |
| 174019 | BAA02g17030 | A02 | 8474959 | C | T | upstream_gene_variant | MODIFIER | c.-4442G>A| |
S77 S82 |
| 174020 | BAA02g17040 | A02 | 8476167 | C | T | upstream_gene_variant | MODIFIER | c.-3782C>T| |
S9 |
| 174021 | BAA02g17040 | A02 | 8477807 | C | T | upstream_gene_variant | MODIFIER | c.-2142C>T| |
S15 S3 |
| 174022 | BAA02g17040 | A02 | 8479094 | C | T | upstream_gene_variant | MODIFIER | c.-855C>T| |
S281 |
| 174023 | BAA02g17040 | A02 | 8479171 | G | A | upstream_gene_variant | MODIFIER | c.-778G>A| |
S17 |
| 174024 | BAA02g17040 | A02 | 8479210 | C | T | upstream_gene_variant | MODIFIER | c.-739C>T| |
S1 S90 |
| 174025 | BAA02g17040 | A02 | 8480700 | G | A | intron_variant | MODIFIER | c.332+420G>A| |
S69 |