| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 129301 | BAA10g17200 | A10 | 16676294 | C | T | upstream_gene_variant | MODIFIER | c.-1509C>T| |
S283 |
| 129302 | BAA10g17200 | A10 | 16676492 | C | T | upstream_gene_variant | MODIFIER | c.-1311C>T| |
S189 |
| 129303 | BAA10g17200 | A10 | 16676854 | G | A | upstream_gene_variant | MODIFIER | c.-949G>A| |
S197 |
| 129304 | BAA10g17200 | A10 | 16677259 | C | T | upstream_gene_variant | MODIFIER | c.-544C>T| |
S121 |
| 129305 | BAA10g17200 | A10 | 16678174 | G | A | synonymous_variant | LOW | c.294G>A|p.Gln98Gln |
S295 |
| 129306 | BAA10g17210 | A10 | 16678842 | G | A | upstream_gene_variant | MODIFIER | c.-1908G>A| |
S291 |
| 129307 | BAA10g17200 | A10 | 16679239 | G | A | missense_variant | MODERATE | c.1021G>A|p.Val341Ile |
S80 |
| 129308 | BAA10g17200 | A10 | 16679674 | G | A | synonymous_variant | LOW | c.1368G>A|p.Lys456Lys |
S283 |
| 129309 | BAA10g17200 | A10 | 16680108 | C | T | synonymous_variant | LOW | c.1618C>T|p.Leu540Leu |
S37 |
| 129310 | BAA10g17210 | A10 | 16680248 | C | T | upstream_gene_variant | MODIFIER | c.-502C>T| |
S37 |
| 129311 | BAA10g17210 | A10 | 16681620 | C | T | missense_variant | MODERATE | c.685C>T|p.Pro229Ser |
S275 |
| 129312 | BAA10g17220 | A10 | 16683182 | G | A | upstream_gene_variant | MODIFIER | c.-3270G>A| |
S69 |
| 129313 | BAA10g17220 | A10 | 16685336 | C | T | upstream_gene_variant | MODIFIER | c.-1116C>T| |
S302 |
| 129314 | BAA10g17220 | A10 | 16686634 | C | T | synonymous_variant | LOW | c.183C>T|p.Phe61Phe |
S133 |
| 129315 | BAA10g17220 | A10 | 16687787 | C | T | missense_variant | MODERATE | c.1336C>T|p.Leu446Phe |
S271 |
| 129316 | BAA10g17220 | A10 | 16687927 | G | A | synonymous_variant | LOW | c.1476G>A|p.Arg492Arg |
S128 |
| 129317 | BAA10g17220 | A10 | 16688075 | G | A | missense_variant | MODERATE | c.1624G>A|p.Glu542Lys |
S245 |
| 129318 | BAA10g17220 | A10 | 16688445 | G | A | downstream_gene_variant | MODIFIER | c.*200G>A| |
S95 |
| 129319 | BAA10g17220 | A10 | 16688504 | G | A | downstream_gene_variant | MODIFIER | c.*259G>A| |
S80 |
| 129320 | BAA10g17230 | A10 | 16688773 | G | A | splice_region_variant&intron_variant | LOW | c.309-7C>T| |
S295 |
| 129321 | BAA10g17230 | A10 | 16689751 | G | A | missense_variant | MODERATE | c.37C>T|p.Leu13Phe |
S111 |
| 129322 | BAA10g17240 | A10 | 16690903 | G | A | missense_variant | MODERATE | c.464C>T|p.Thr155Ile |
S128 |
| 129323 | BAA10g17240 | A10 | 16696543 | C | T | upstream_gene_variant | MODIFIER | c.-4636G>A| |
S2 S213 S4 S6 |
| 129324 | BAA10g17250 | A10 | 16699966 | C | T | upstream_gene_variant | MODIFIER | c.-699G>A| |
S18 |
| 129325 | BAA10g17260 | A10 | 16700715 | C | T | missense_variant | MODERATE | c.166C>T|p.Pro56Ser |
S238 |