| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 116401 | BAA10g10240 | A10 | 12013368 | C | T | downstream_gene_variant | MODIFIER | c.*858G>A| |
S236 |
| 116402 | BAA10g10240 | A10 | 12013832 | C | T | downstream_gene_variant | MODIFIER | c.*394G>A| |
S256 |
| 116403 | BAA10g10240 | A10 | 12014075 | C | T | downstream_gene_variant | MODIFIER | c.*151G>A| |
S174 S27 |
| 116404 | BAA10g10240 | A10 | 12014395 | C | T | intron_variant | MODIFIER | c.514-26G>A| |
S177 |
| 116405 | BAA10g10250 | A10 | 12016775 | G | A | upstream_gene_variant | MODIFIER | c.-4599G>A| |
S94 |
| 116406 | BAA10g10250 | A10 | 12017428 | G | A | upstream_gene_variant | MODIFIER | c.-3946G>A| |
S217 S248 |
| 116407 | BAA10g10250 | A10 | 12019369 | G | A | upstream_gene_variant | MODIFIER | c.-2005G>A| |
S107 |
| 116408 | BAA10g10240 | A10 | 12019625 | G | A | missense_variant | MODERATE | c.179C>T|p.Ser60Phe |
S289 |
| 116409 | BAA10g10240 | A10 | 12019909 | G | A | upstream_gene_variant | MODIFIER | c.-106C>T| |
S69 |
| 116410 | BAA10g10240 | A10 | 12020065 | G | A | upstream_gene_variant | MODIFIER | c.-262C>T| |
S13 |
| 116411 | BAA10g10240 | A10 | 12020256 | G | A | upstream_gene_variant | MODIFIER | c.-453C>T| |
S71 |
| 116412 | BAA10g10240 | A10 | 12020596 | C | T | upstream_gene_variant | MODIFIER | c.-793G>A| |
S152 |
| 116413 | BAA10g10240 | A10 | 12021004 | C | T | upstream_gene_variant | MODIFIER | c.-1201G>A| |
S46 |
| 116414 | BAA10g10250 | A10 | 12021533 | G | A | missense_variant&splice_region_variant | MODERATE | c.160G>A|p.Gly54Arg |
S4 |
| 116415 | BAA10g10240 | A10 | 12022030 | G | A | upstream_gene_variant | MODIFIER | c.-2227C>T| |
S240 |
| 116416 | BAA10g10240 | A10 | 12022141 | C | T | upstream_gene_variant | MODIFIER | c.-2338G>A| |
S187 |
| 116417 | BAA10g10240 | A10 | 12022828 | G | A | upstream_gene_variant | MODIFIER | c.-3025C>T| |
S78 |
| 116418 | BAA10g10260 | A10 | 12023828 | G | A | missense_variant | MODERATE | c.995C>T|p.Thr332Met |
S217 S248 |
| 116419 | BAA10g10260 | A10 | 12023900 | C | T | missense_variant | MODERATE | c.923G>A|p.Gly308Glu |
S38 |
| 116420 | BAA10g10260 | A10 | 12023955 | C | T | missense_variant | MODERATE | c.868G>A|p.Val290Met |
S249 |
| 116421 | BAA10g10240 | A10 | 12024522 | C | T | upstream_gene_variant | MODIFIER | c.-4719G>A| |
S260 |
| 116422 | BAA10g10260 | A10 | 12025232 | G | A | missense_variant | MODERATE | c.239C>T|p.Thr80Ile |
S216 |
| 116423 | BAA10g10260 | A10 | 12026352 | G | A | upstream_gene_variant | MODIFIER | c.-810C>T| |
S127 |
| 116424 | BAA10g10260 | A10 | 12026945 | G | A | upstream_gene_variant | MODIFIER | c.-1403C>T| |
S293 |
| 116425 | BAA10g10260 | A10 | 12027481 | G | A | upstream_gene_variant | MODIFIER | c.-1939C>T| |
S69 |