| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 10101 | BAA01g08260 | A01 | 3615563 | G | A | missense_variant | MODERATE | c.1259G>A|p.Arg420Lys |
S234 |
| 10102 | BAA01g08260 | A01 | 3615788 | G | A | synonymous_variant | LOW | c.1401G>A|p.Glu467Glu |
S187 |
| 10103 | BAA01g08260 | A01 | 3615852 | C | T | missense_variant | MODERATE | c.1465C>T|p.Pro489Ser |
S153 S213 |
| 10104 | BAA01g08260 | A01 | 3615922 | G | A | splice_donor_variant&intron_variant | HIGH | c.1534+1G>A| |
S69 |
| 10105 | BAA01g08260 | A01 | 3616344 | C | T | missense_variant | MODERATE | c.1780C>T|p.Pro594Ser |
S263 |
| 10106 | BAA01g08260 | A01 | 3616889 | G | T | missense_variant | MODERATE | c.2240G>T|p.Arg747Ile |
S149 |
| 10107 | BAA01g08260 | A01 | 3616911 | G | A | missense_variant | MODERATE | c.2262G>A|p.Met754Ile |
S151 S202 |
| 10108 | BAA01g08260 | A01 | 3617648 | G | A | missense_variant | MODERATE | c.2842G>A|p.Val948Ile |
S202 |
| 10109 | BAA01g08260 | A01 | 3617671 | G | A | downstream_gene_variant | MODIFIER | c.*18G>A| |
S204 |
| 10110 | BAA01g08260 | A01 | 3617831 | C | T | downstream_gene_variant | MODIFIER | c.*178C>T| |
S43 |
| 10111 | BAA01g08260 | A01 | 3618034 | G | A | downstream_gene_variant | MODIFIER | c.*381G>A| |
S195 |
| 10112 | BAA01g08260 | A01 | 3618205 | C | T | downstream_gene_variant | MODIFIER | c.*552C>T| |
S166 |
| 10113 | BAA01g08260 | A01 | 3618347 | C | T | downstream_gene_variant | MODIFIER | c.*694C>T| |
S128 |
| 10114 | BAA01g08260 | A01 | 3618850 | C | T | downstream_gene_variant | MODIFIER | c.*1197C>T| |
S18 |
| 10115 | BAA01g08260 | A01 | 3619139 | G | A | downstream_gene_variant | MODIFIER | c.*1486G>A| |
S216 |
| 10116 | BAA01g08270 | A01 | 3620221 | C | T | upstream_gene_variant | MODIFIER | c.-593G>A| |
S164 |
| 10117 | BAA01g08270 | A01 | 3621033 | G | A | upstream_gene_variant | MODIFIER | c.-1405C>T| |
S294 |
| 10118 | BAA01g08270 | A01 | 3621425 | G | A | upstream_gene_variant | MODIFIER | c.-1797C>T| |
S186 |
| 10119 | BAA01g08270 | A01 | 3621478 | G | A | upstream_gene_variant | MODIFIER | c.-1850C>T| |
S293 |
| 10120 | BAA01g08270 | A01 | 3622239 | G | A | upstream_gene_variant | MODIFIER | c.-2611C>T| |
S287 |
| 10121 | BAA01g08270 | A01 | 3622829 | G | A | upstream_gene_variant | MODIFIER | c.-3201C>T| |
S115 |
| 10122 | BAA01g08270 | A01 | 3622862 | G | A | upstream_gene_variant | MODIFIER | c.-3234C>T| |
S116 |
| 10123 | BAA01g08270 | A01 | 3624146 | C | T | upstream_gene_variant | MODIFIER | c.-4518G>A| |
S1 S90 |
| 10124 | BAA01g08270 | A01 | 3624441 | G | A | upstream_gene_variant | MODIFIER | c.-4813C>T| |
S118 |
| 10125 | BAA01g08280 | A01 | 3624559 | G | T | missense_variant | MODERATE | c.710C>A|p.Pro237His |
S133 |