| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 147301 | BAA10g31700 | A10 | 23045134 | C | T | missense_variant | MODERATE | c.778G>A|p.Asp260Asn |
S230 |
| 147302 | BAA10g31700 | A10 | 23046474 | C | T | upstream_gene_variant | MODIFIER | c.-334G>A| |
S129 |
| 147303 | BAA10g31700 | A10 | 23046540 | C | T | upstream_gene_variant | MODIFIER | c.-400G>A| |
S90 |
| 147304 | BAA10g31710 | A10 | 23047627 | G | A | missense_variant | MODERATE | c.334G>A|p.Glu112Lys |
S276 |
| 147305 | BAA10g31710 | A10 | 23047846 | G | A | missense_variant | MODERATE | c.553G>A|p.Glu185Lys |
S298 |
| 147306 | BAA10g31700 | A10 | 23048102 | G | A | upstream_gene_variant | MODIFIER | c.-1962C>T| |
S151 |
| 147307 | BAA10g31700 | A10 | 23048519 | C | T | upstream_gene_variant | MODIFIER | c.-2379G>A| |
S25 |
| 147308 | BAA10g31710 | A10 | 23048948 | C | T | missense_variant | MODERATE | c.979C>T|p.Leu327Phe |
S269 |
| 147309 | BAA10g31710 | A10 | 23048991 | G | A | missense_variant | MODERATE | c.1022G>A|p.Arg341Lys |
S237 |
| 147310 | BAA10g31700 | A10 | 23049562 | G | A | upstream_gene_variant | MODIFIER | c.-3422C>T| |
S217 |
| 147311 | BAA10g31700 | A10 | 23049701 | C | T | upstream_gene_variant | MODIFIER | c.-3561G>A| |
S12 |
| 147312 | BAA10g31700 | A10 | 23049866 | G | A | upstream_gene_variant | MODIFIER | c.-3726C>T| |
S171 |
| 147313 | BAA10g31720 | A10 | 23051346 | C | T | upstream_gene_variant | MODIFIER | c.-1139C>T| |
S11 |
| 147314 | BAA10g31720 | A10 | 23051678 | G | A | upstream_gene_variant | MODIFIER | c.-807G>A| |
S207 |
| 147315 | BAA10g31720 | A10 | 23052442 | C | T | upstream_gene_variant | MODIFIER | c.-43C>T| |
S20 |
| 147316 | BAA10g31740 | A10 | 23055156 | C | T | upstream_gene_variant | MODIFIER | c.-2443C>T| |
S272 |
| 147317 | BAA10g31740 | A10 | 23055665 | C | T | upstream_gene_variant | MODIFIER | c.-1934C>T| |
S283 |
| 147318 | BAA10g31740 | A10 | 23057694 | C | T | synonymous_variant | LOW | c.96C>T|p.Leu32Leu |
S45 |
| 147319 | BAA10g31740 | A10 | 23059219 | C | T | missense_variant | MODERATE | c.767C>T|p.Ala256Val |
S33 |
| 147320 | BAA10g31740 | A10 | 23059372 | C | T | missense_variant | MODERATE | c.809C>T|p.Ala270Val |
S195 |
| 147321 | BAA10g31730 | A10 | 23059813 | G | A | upstream_gene_variant | MODIFIER | c.-3758C>T| |
S158 |
| 147322 | BAA10g31730 | A10 | 23060007 | G | A | upstream_gene_variant | MODIFIER | c.-3952C>T| |
S250 |
| 147323 | BAA10g31730 | A10 | 23060514 | C | T | upstream_gene_variant | MODIFIER | c.-4459G>A| |
S140 |
| 147324 | BAA10g31750 | A10 | 23066713 | G | A | stop_gained | HIGH | c.1138C>T|p.Gln380* |
S279 |
| 147325 | BAA10g31750 | A10 | 23067266 | G | A | synonymous_variant | LOW | c.585C>T|p.Leu195Leu |
S240 |