| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 130201 | BAA10g17800 | A10 | 16986402 | G | A | upstream_gene_variant | MODIFIER | c.-1693G>A| |
S192 |
| 130202 | BAA10g17800 | A10 | 16987121 | C | T | upstream_gene_variant | MODIFIER | c.-974C>T| |
S73 |
| 130203 | BAA10g17800 | A10 | 16987921 | C | T | upstream_gene_variant | MODIFIER | c.-174C>T| |
S11 |
| 130204 | BAA10g17810 | A10 | 16988915 | C | T | downstream_gene_variant | MODIFIER | c.*2738G>A| |
S231 |
| 130205 | BAA10g17810 | A10 | 16989083 | C | T | downstream_gene_variant | MODIFIER | c.*2570G>A| |
S84 S93 |
| 130206 | BAA10g17800 | A10 | 16989115 | G | A | synonymous_variant | LOW | c.627G>A|p.Glu209Glu |
S32 |
| 130207 | BAA10g17810 | A10 | 16989575 | C | T | downstream_gene_variant | MODIFIER | c.*2078G>A| |
S305 |
| 130208 | BAA10g17810 | A10 | 16990055 | C | T | downstream_gene_variant | MODIFIER | c.*1598G>A| |
S117 |
| 130209 | BAA10g17810 | A10 | 16990317 | G | A | downstream_gene_variant | MODIFIER | c.*1336C>T| |
S261 |
| 130210 | BAA10g17800 | A10 | 16990903 | G | A | downstream_gene_variant | MODIFIER | c.*72G>A| |
S273 |
| 130211 | BAA10g17800 | A10 | 16990936 | A | C | downstream_gene_variant | MODIFIER | c.*105A>C| |
S114 S168 S169 S183 S225 S270 S297 |
| 130212 | BAA10g17830 | A10 | 16991131 | G | A | upstream_gene_variant | MODIFIER | c.-4895G>A| |
S166 |
| 130213 | BAA10g17810 | A10 | 16992445 | C | T | missense_variant | MODERATE | c.199G>A|p.Glu67Lys |
S107 |
| 130214 | BAA10g17810 | A10 | 16994375 | G | A | upstream_gene_variant | MODIFIER | c.-1574C>T| |
S138 |
| 130215 | BAA10g17830 | A10 | 16996594 | C | T | synonymous_variant | LOW | c.388C>T|p.Leu130Leu |
S226 |
| 130216 | BAA10g17810 | A10 | 16997332 | C | T | upstream_gene_variant | MODIFIER | c.-4531G>A| |
S95 |
| 130217 | BAA10g17840 | A10 | 16999204 | C | T | missense_variant | MODERATE | c.1316C>T|p.Ser439Phe |
S242 |
| 130218 | BAA10g17840 | A10 | 16999261 | C | T | missense_variant | MODERATE | c.1373C>T|p.Ser458Phe |
S199 |
| 130219 | BAA10g17830 | A10 | 17000601 | C | T | downstream_gene_variant | MODIFIER | c.*3515C>T| |
S33 |
| 130220 | BAA10g17830 | A10 | 17001633 | C | T | downstream_gene_variant | MODIFIER | c.*4547C>T| |
S283 |
| 130221 | BAA10g17830 | A10 | 17001884 | C | T | downstream_gene_variant | MODIFIER | c.*4798C>T| |
S249 |
| 130222 | BAA10g17850 | A10 | 17005812 | G | A | missense_variant | MODERATE | c.920C>T|p.Ser307Leu |
S130 S240 |
| 130223 | BAA10g17850 | A10 | 17006377 | C | T | missense_variant | MODERATE | c.355G>A|p.Glu119Lys |
S99 |
| 130224 | BAA10g17850 | A10 | 17006844 | G | A | upstream_gene_variant | MODIFIER | c.-113C>T| |
S195 |
| 130225 | BAA10g17850 | A10 | 17007031 | G | A | upstream_gene_variant | MODIFIER | c.-300C>T| |
S166 |