| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 114151 | BAA10g09170 | A10 | 11213566 | G | A | upstream_gene_variant | MODIFIER | c.-3440G>A| |
S8 |
| 114152 | BAA10g09170 | A10 | 11214285 | C | T | upstream_gene_variant | MODIFIER | c.-2721C>T| |
S177 |
| 114153 | BAA10g09170 | A10 | 11215541 | G | A | upstream_gene_variant | MODIFIER | c.-1465G>A| |
S176 |
| 114154 | BAA10g09170 | A10 | 11216036 | G | A | upstream_gene_variant | MODIFIER | c.-970G>A| |
S107 |
| 114155 | BAA10g09170 | A10 | 11216117 | G | A | upstream_gene_variant | MODIFIER | c.-889G>A| |
S221 |
| 114156 | BAA10g09170 | A10 | 11217087 | G | A | missense_variant | MODERATE | c.82G>A|p.Glu28Lys |
S151 S263 |
| 114157 | BAA10g09180 | A10 | 11218417 | G | A | upstream_gene_variant | MODIFIER | c.-3249G>A| |
S85 S90 |
| 114158 | BAA10g09180 | A10 | 11219246 | C | T | upstream_gene_variant | MODIFIER | c.-2420C>T| |
S149 |
| 114159 | BAA10g09180 | A10 | 11219911 | C | T | upstream_gene_variant | MODIFIER | c.-1755C>T| |
S291 |
| 114160 | BAA10g09180 | A10 | 11219925 | C | A | upstream_gene_variant | MODIFIER | c.-1741C>A| |
S17 S184 S218 S268 S269 |
| 114161 | BAA10g09180 | A10 | 11220529 | G | A | upstream_gene_variant | MODIFIER | c.-1137G>A| |
S274 |
| 114162 | BAA10g09180 | A10 | 11221485 | C | T | upstream_gene_variant | MODIFIER | c.-181C>T| |
S204 |
| 114163 | BAA10g09180 | A10 | 11221769 | C | T | missense_variant | MODERATE | c.104C>T|p.Ser35Phe |
S195 |
| 114164 | BAA10g09190 | A10 | 11221873 | G | A | upstream_gene_variant | MODIFIER | c.-1699G>A| |
S286 |
| 114165 | BAA10g09190 | A10 | 11223609 | C | T | missense_variant | MODERATE | c.38C>T|p.Pro13Leu |
S68 |
| 114166 | BAA10g09190 | A10 | 11223692 | C | T | missense_variant | MODERATE | c.121C>T|p.Arg41Cys |
S308 |
| 114167 | BAA10g09170 | A10 | 11223934 | G | A | downstream_gene_variant | MODIFIER | c.*4909G>A| |
S67 |
| 114168 | BAA10g09190 | A10 | 11224804 | G | A | missense_variant | MODERATE | c.931G>A|p.Ala311Thr |
S245 |
| 114169 | BAA10g09190 | A10 | 11224815 | G | A | synonymous_variant | LOW | c.942G>A|p.Lys314Lys |
S9 |
| 114170 | BAA10g09190 | A10 | 11224970 | C | T | splice_region_variant&intron_variant | LOW | c.1006-7C>T| |
S153 S213 |
| 114171 | BAA10g09190 | A10 | 11225236 | C | T | missense_variant | MODERATE | c.1172C>T|p.Ala391Val |
S174 S27 |
| 114172 | BAA10g09210 | A10 | 11226580 | C | T | upstream_gene_variant | MODIFIER | c.-4914C>T| |
S167 |
| 114173 | BAA10g09200 | A10 | 11226867 | C | T | missense_variant | MODERATE | c.776G>A|p.Gly259Asp |
S168 S279 S64 |
| 114174 | BAA10g09200 | A10 | 11227122 | A | C | missense_variant | MODERATE | c.627T>G|p.Asp209Glu |
S64 |
| 114175 | BAA10g09200 | A10 | 11227300 | C | T | stop_gained | HIGH | c.519G>A|p.Trp173* |
S126 |