| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 146351 | BAA10g30800 | A10 | 22702546 | G | A | missense_variant | MODERATE | c.1115C>T|p.Ser372Phe |
S109 |
| 146352 | BAA10g30800 | A10 | 22703652 | G | A | synonymous_variant | LOW | c.9C>T|p.Asn3Asn |
S32 |
| 146353 | BAA10g30800 | A10 | 22705498 | G | A | upstream_gene_variant | MODIFIER | c.-1838C>T| |
S38 |
| 146354 | BAA10g30800 | A10 | 22705858 | G | A | upstream_gene_variant | MODIFIER | c.-2198C>T| |
S202 |
| 146355 | BAA10g30800 | A10 | 22706015 | C | T | upstream_gene_variant | MODIFIER | c.-2355G>A| |
S34 |
| 146356 | BAA10g30800 | A10 | 22706048 | G | A | upstream_gene_variant | MODIFIER | c.-2388C>T| |
S38 |
| 146357 | BAA10g30800 | A10 | 22706201 | C | T | upstream_gene_variant | MODIFIER | c.-2541G>A| |
S287 |
| 146358 | BAA10g30810 | A10 | 22707091 | C | T | missense_variant | MODERATE | c.196G>A|p.Asp66Asn |
S42 |
| 146359 | BAA10g30820 | A10 | 22709228 | G | A | missense_variant | MODERATE | c.79G>A|p.Gly27Arg |
S265 |
| 146360 | BAA10g30820 | A10 | 22710199 | G | A | missense_variant | MODERATE | c.665G>A|p.Ser222Asn |
S118 |
| 146361 | BAA10g30820 | A10 | 22710547 | C | T | missense_variant | MODERATE | c.1013C>T|p.Thr338Ile |
S164 |
| 146362 | BAA10g30810 | A10 | 22711662 | C | T | upstream_gene_variant | MODIFIER | c.-4376G>A| |
S190 |
| 146363 | BAA10g30810 | A10 | 22711983 | C | T | upstream_gene_variant | MODIFIER | c.-4697G>A| |
S177 |
| 146364 | BAA10g30810 | A10 | 22712189 | A | T | upstream_gene_variant | MODIFIER | c.-4903T>A| |
S11 |
| 146365 | BAA10g30830 | A10 | 22712548 | G | A | upstream_gene_variant | MODIFIER | c.-413G>A| |
S284 |
| 146366 | BAA10g30850 | A10 | 22713251 | C | T | upstream_gene_variant | MODIFIER | c.-4914C>T| |
S161 |
| 146367 | BAA10g30830 | A10 | 22713391 | A | T | missense_variant | MODERATE | c.346A>T|p.Ile116Phe |
S259 |
| 146368 | BAA10g30840 | A10 | 22714316 | C | T | splice_region_variant&intron_variant | LOW | c.3130+8G>A| |
S283 |
| 146369 | BAA10g30840 | A10 | 22714567 | G | A | missense_variant | MODERATE | c.2887C>T|p.Arg963Cys |
S80 |
| 146370 | BAA10g30840 | A10 | 22714704 | C | T | missense_variant | MODERATE | c.2750G>A|p.Gly917Asp |
S144 |
| 146371 | BAA10g30840 | A10 | 22714980 | C | T | missense_variant | MODERATE | c.2474G>A|p.Arg825Lys |
S153 S213 |
| 146372 | BAA10g30840 | A10 | 22715414 | G | A | synonymous_variant | LOW | c.2040C>T|p.Leu680Leu |
S259 |
| 146373 | BAA10g30840 | A10 | 22719349 | G | A | upstream_gene_variant | MODIFIER | c.-1896C>T| |
S76 |
| 146374 | BAA10g30840 | A10 | 22719568 | C | T | upstream_gene_variant | MODIFIER | c.-2115G>A| |
S268 |
| 146375 | BAA10g30840 | A10 | 22719622 | G | A | upstream_gene_variant | MODIFIER | c.-2169C>T| |
S149 |