| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 121201 | BAA10g12230 | A10 | 13680245 | G | A | downstream_gene_variant | MODIFIER | c.*4852C>T| |
S159 S243 |
| 121202 | BAA10g12230 | A10 | 13681105 | C | T | downstream_gene_variant | MODIFIER | c.*3992G>A| |
S256 |
| 121203 | BAA10g12230 | A10 | 13681316 | G | A | downstream_gene_variant | MODIFIER | c.*3781C>T| |
S67 |
| 121204 | BAA10g12230 | A10 | 13682748 | G | A | downstream_gene_variant | MODIFIER | c.*2349C>T| |
S158 |
| 121205 | BAA10g12230 | A10 | 13685365 | C | T | missense_variant | MODERATE | c.704G>A|p.Arg235His |
S244 |
| 121206 | BAA10g12230 | A10 | 13685508 | G | A | intron_variant | MODIFIER | c.619+30C>T| |
S178 |
| 121207 | BAA10g12230 | A10 | 13685594 | G | A | missense_variant | MODERATE | c.563C>T|p.Pro188Leu |
S302 |
| 121208 | BAA10g12230 | A10 | 13685660 | G | A | missense_variant | MODERATE | c.497C>T|p.Ser166Leu |
S64 |
| 121209 | BAA10g12230 | A10 | 13686970 | C | T | upstream_gene_variant | MODIFIER | c.-814G>A| |
S247 |
| 121210 | BAA10g12230 | A10 | 13688831 | G | A | upstream_gene_variant | MODIFIER | c.-2675C>T| |
S279 |
| 121211 | BAA10g12230 | A10 | 13689257 | G | A | upstream_gene_variant | MODIFIER | c.-3101C>T| |
S186 |
| 121212 | BAA10g12230 | A10 | 13689497 | G | A | upstream_gene_variant | MODIFIER | c.-3341C>T| |
S34 |
| 121213 | BAA10g12230 | A10 | 13690326 | A | G | upstream_gene_variant | MODIFIER | c.-4170T>C| |
S56 |
| 121214 | BAA10g12230 | A10 | 13691055 | G | A | upstream_gene_variant | MODIFIER | c.-4899C>T| |
S81 |
| 121215 | BAA10g12230 | A10 | 13691059 | C | T | upstream_gene_variant | MODIFIER | c.-4903G>A| |
S114 |
| 121216 | BAA10g12240 | A10 | 13691680 | G | A | downstream_gene_variant | MODIFIER | c.*647C>T| |
S107 |
| 121217 | BAA10g12240 | A10 | 13692187 | C | T | downstream_gene_variant | MODIFIER | c.*140G>A| |
S249 |
| 121218 | BAA10g12240 | A10 | 13692365 | C | T | missense_variant | MODERATE | c.412G>A|p.Gly138Arg |
S270 |
| 121219 | BAA10g12250 | A10 | 13693390 | A | G | downstream_gene_variant | MODIFIER | c.*903T>C| |
S20 |
| 121220 | BAA10g12240 | A10 | 13694165 | C | T | upstream_gene_variant | MODIFIER | c.-705G>A| |
S76 |
| 121221 | BAA10g12250 | A10 | 13694571 | C | T | missense_variant&splice_region_variant | MODERATE | c.1253G>A|p.Ser418Asn |
S162 |
| 121222 | BAA10g12240 | A10 | 13695088 | G | A | upstream_gene_variant | MODIFIER | c.-1628C>T| |
S13 |
| 121223 | BAA10g12240 | A10 | 13695936 | C | T | upstream_gene_variant | MODIFIER | c.-2476G>A| |
S246 |
| 121224 | BAA10g12250 | A10 | 13696053 | G | A | synonymous_variant | LOW | c.555C>T|p.Pro185Pro |
S205 S39 |
| 121225 | BAA10g12250 | A10 | 13696103 | G | A | stop_gained | HIGH | c.505C>T|p.Gln169* |
S219 S72 |