| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 139001 | BAA10g24380 | A10 | 20108162 | C | T | upstream_gene_variant | MODIFIER | c.-4000G>A| |
S169 |
| 139002 | BAA10g24380 | A10 | 20108592 | G | A | upstream_gene_variant | MODIFIER | c.-4430C>T| |
S202 |
| 139003 | BAA10g24390 | A10 | 20109608 | C | T | upstream_gene_variant | MODIFIER | c.-2409C>T| |
S282 |
| 139004 | BAA10g24390 | A10 | 20109826 | G | A | upstream_gene_variant | MODIFIER | c.-2191G>A| |
S198 |
| 139005 | BAA10g24390 | A10 | 20110127 | C | T | upstream_gene_variant | MODIFIER | c.-1890C>T| |
S244 |
| 139006 | BAA10g24390 | A10 | 20110198 | C | T | upstream_gene_variant | MODIFIER | c.-1819C>T| |
S47 |
| 139007 | BAA10g24390 | A10 | 20110403 | C | T | upstream_gene_variant | MODIFIER | c.-1614C>T| |
S195 |
| 139008 | BAA10g24390 | A10 | 20110723 | G | A | upstream_gene_variant | MODIFIER | c.-1294G>A| |
S209 |
| 139009 | BAA10g24390 | A10 | 20112147 | G | T | missense_variant | MODERATE | c.131G>T|p.Gly44Val |
S134 |
| 139010 | BAA10g24390 | A10 | 20113164 | C | T | missense_variant | MODERATE | c.764C>T|p.Thr255Met |
S292 |
| 139011 | BAA10g24390 | A10 | 20114387 | C | T | synonymous_variant | LOW | c.1917C>T|p.Val639Val |
S103 |
| 139012 | BAA10g24390 | A10 | 20114757 | C | T | synonymous_variant | LOW | c.2199C>T|p.Phe733Phe |
S96 |
| 139013 | BAA10g24410 | A10 | 20115881 | G | A | upstream_gene_variant | MODIFIER | c.-1967G>A| |
S150 |
| 139014 | BAA10g24400 | A10 | 20116091 | C | T | missense_variant | MODERATE | c.1003G>A|p.Gly335Ser |
S108 |
| 139015 | BAA10g24400 | A10 | 20116736 | G | A | missense_variant | MODERATE | c.358C>T|p.Leu120Phe |
S173 |
| 139016 | BAA10g24400 | A10 | 20117220 | C | T | upstream_gene_variant | MODIFIER | c.-127G>A| |
S275 |
| 139017 | BAA10g24400 | A10 | 20117334 | C | T | upstream_gene_variant | MODIFIER | c.-241G>A| |
S269 |
| 139018 | BAA10g24400 | A10 | 20117679 | C | A | upstream_gene_variant | MODIFIER | c.-586G>T| |
S204 |
| 139019 | BAA10g24400 | A10 | 20117839 | G | A | upstream_gene_variant | MODIFIER | c.-746C>T| |
S139 |
| 139020 | BAA10g24410 | A10 | 20118302 | G | A | synonymous_variant | LOW | c.300G>A|p.Glu100Glu |
S159 S243 |
| 139021 | BAA10g24410 | A10 | 20118363 | C | T | splice_region_variant&intron_variant | LOW | c.353+8C>T| |
S188 |
| 139022 | BAA10g24400 | A10 | 20119078 | G | A | upstream_gene_variant | MODIFIER | c.-1985C>T| |
S182 |
| 139023 | BAA10g24400 | A10 | 20120806 | C | T | upstream_gene_variant | MODIFIER | c.-3713G>A| |
S133 |
| 139024 | BAA10g24400 | A10 | 20121912 | C | T | upstream_gene_variant | MODIFIER | c.-4819G>A| |
S107 |
| 139025 | BAA10g24420 | A10 | 20123432 | G | A | missense_variant | MODERATE | c.1221G>A|p.Met407Ile |
S217 S248 |