| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 133101 | BAA10g19690 | A10 | 17993468 | G | A | missense_variant | MODERATE | c.490C>T|p.Pro164Ser |
S279 |
| 133102 | BAA10g19690 | A10 | 17995056 | C | T | upstream_gene_variant | MODIFIER | c.-927G>A| |
S189 |
| 133103 | BAA10g19690 | A10 | 17995118 | C | T | upstream_gene_variant | MODIFIER | c.-989G>A| |
S156 |
| 133104 | BAA10g19690 | A10 | 17995565 | C | T | upstream_gene_variant | MODIFIER | c.-1436G>A| |
S199 |
| 133105 | BAA10g19690 | A10 | 17995989 | C | T | upstream_gene_variant | MODIFIER | c.-1860G>A| |
S99 |
| 133106 | BAA10g19690 | A10 | 17997507 | C | T | upstream_gene_variant | MODIFIER | c.-3378G>A| |
S251 |
| 133107 | BAA10g19700 | A10 | 17997598 | C | T | stop_gained | HIGH | c.478C>T|p.Arg160* |
S61 |
| 133108 | BAA10g19700 | A10 | 17999116 | G | A | missense_variant | MODERATE | c.887G>A|p.Arg296Lys |
S287 |
| 133109 | BAA10g19710 | A10 | 18000531 | C | T | missense_variant | MODERATE | c.379G>A|p.Glu127Lys |
S308 |
| 133110 | BAA10g19710 | A10 | 18000582 | C | T | missense_variant | MODERATE | c.328G>A|p.Ala110Thr |
S109 S26 |
| 133111 | BAA10g19710 | A10 | 18001263 | C | T | upstream_gene_variant | MODIFIER | c.-354G>A| |
S117 |
| 133112 | BAA10g19720 | A10 | 18001517 | G | A | missense_variant | MODERATE | c.65G>A|p.Gly22Glu |
S112 |
| 133113 | BAA10g19720 | A10 | 18001872 | C | A | missense_variant | MODERATE | c.420C>A|p.Ser140Arg |
S301 S304 |
| 133114 | BAA10g19720 | A10 | 18001915 | C | T | missense_variant | MODERATE | c.463C>T|p.His155Tyr |
S78 |
| 133115 | BAA10g19720 | A10 | 18002160 | G | A | synonymous_variant | LOW | c.708G>A|p.Thr236Thr |
S59 |
| 133116 | BAA10g19720 | A10 | 18002885 | G | A | missense_variant | MODERATE | c.1433G>A|p.Gly478Glu |
S71 |
| 133117 | BAA10g19720 | A10 | 18002958 | C | T | synonymous_variant | LOW | c.1506C>T|p.Asp502Asp |
S19 |
| 133118 | BAA10g19710 | A10 | 18003385 | G | A | upstream_gene_variant | MODIFIER | c.-2476C>T| |
S303 |
| 133119 | BAA10g19710 | A10 | 18004452 | G | A | upstream_gene_variant | MODIFIER | c.-3543C>T| |
S57 |
| 133120 | BAA10g19710 | A10 | 18005048 | G | A | upstream_gene_variant | MODIFIER | c.-4139C>T| |
S175 |
| 133121 | BAA10g19710 | A10 | 18005200 | G | A | upstream_gene_variant | MODIFIER | c.-4291C>T| |
S25 |
| 133122 | BAA10g19710 | A10 | 18005734 | C | T | upstream_gene_variant | MODIFIER | c.-4825G>A| |
S143 |
| 133123 | BAA10g19730 | A10 | 18006328 | G | A | missense_variant | MODERATE | c.214G>A|p.Glu72Lys |
S240 |
| 133124 | BAA10g19730 | A10 | 18007870 | C | T | synonymous_variant | LOW | c.1248C>T|p.Arg416Arg |
S10 |
| 133125 | BAA10g19730 | A10 | 18008700 | C | T | missense_variant | MODERATE | c.1715C>T|p.Thr572Ile |
S200 |