| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 126251 | BAA10g15060 | A10 | 15589702 | C | T | upstream_gene_variant | MODIFIER | c.-1508G>A| |
S256 |
| 126252 | BAA10g15060 | A10 | 15589751 | G | A | upstream_gene_variant | MODIFIER | c.-1557C>T| |
S209 |
| 126253 | BAA10g15060 | A10 | 15589975 | G | A | upstream_gene_variant | MODIFIER | c.-1781C>T| |
S182 |
| 126254 | BAA10g15070 | A10 | 15592974 | G | A | missense_variant | MODERATE | c.362G>A|p.Arg121Lys |
S129 |
| 126255 | BAA10g15070 | A10 | 15593169 | G | A | missense_variant | MODERATE | c.487G>A|p.Ala163Thr |
S286 |
| 126256 | BAA10g15080 | A10 | 15593611 | G | A | downstream_gene_variant | MODIFIER | c.*2628C>T| |
S112 |
| 126257 | BAA10g15070 | A10 | 15594148 | G | A | missense_variant | MODERATE | c.964G>A|p.Glu322Lys |
S272 |
| 126258 | BAA10g15070 | A10 | 15594166 | C | T | missense_variant | MODERATE | c.982C>T|p.Pro328Ser |
S37 |
| 126259 | BAA10g15080 | A10 | 15594842 | G | A | downstream_gene_variant | MODIFIER | c.*1397C>T| |
S139 |
| 126260 | BAA10g15070 | A10 | 15595304 | C | T | missense_variant | MODERATE | c.1739C>T|p.Ser580Phe |
S259 |
| 126261 | BAA10g15070 | A10 | 15595546 | G | A | downstream_gene_variant | MODIFIER | c.*202G>A| |
S120 |
| 126262 | BAA10g15080 | A10 | 15596665 | C | T | stop_gained | HIGH | c.1914G>A|p.Trp638* |
S302 |
| 126263 | BAA10g15080 | A10 | 15597053 | C | T | missense_variant | MODERATE | c.1526G>A|p.Ser509Asn |
S297 |
| 126264 | BAA10g15080 | A10 | 15597093 | G | A | missense_variant | MODERATE | c.1486C>T|p.Pro496Ser |
S271 |
| 126265 | BAA10g15080 | A10 | 15597553 | C | T | synonymous_variant | LOW | c.1026G>A|p.Leu342Leu |
S124 |
| 126266 | BAA10g15080 | A10 | 15597939 | C | T | missense_variant | MODERATE | c.640G>A|p.Glu214Lys |
S11 |
| 126267 | BAA10g15080 | A10 | 15598933 | C | T | missense_variant | MODERATE | c.104G>A|p.Gly35Glu |
S117 |
| 126268 | BAA10g15090 | A10 | 15600345 | C | T | missense_variant | MODERATE | c.313G>A|p.Val105Ile |
S297 |
| 126269 | BAA10g15090 | A10 | 15600427 | G | A | synonymous_variant | LOW | c.231C>T|p.Pro77Pro |
S192 |
| 126270 | BAA10g15080 | A10 | 15600503 | C | T | upstream_gene_variant | MODIFIER | c.-1467G>A| |
S210 |
| 126271 | BAA10g15080 | A10 | 15600913 | G | A | upstream_gene_variant | MODIFIER | c.-1877C>T| |
S241 |
| 126272 | BAA10g15080 | A10 | 15602795 | G | A | upstream_gene_variant | MODIFIER | c.-3759C>T| |
S139 |
| 126273 | BAA10g15090 | A10 | 15604676 | C | T | upstream_gene_variant | MODIFIER | c.-3919G>A| |
S87 |
| 126274 | BAA10g15090 | A10 | 15605389 | G | A | upstream_gene_variant | MODIFIER | c.-4632C>T| |
S30 S31 |
| 126275 | BAA10g15090 | A10 | 15605558 | G | A | upstream_gene_variant | MODIFIER | c.-4801C>T| |
S105 S106 |