| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 131351 | BAA10g18610 | A10 | 17381440 | C | T | upstream_gene_variant | MODIFIER | c.-445G>A| |
S189 |
| 131352 | BAA10g18610 | A10 | 17381831 | G | A | upstream_gene_variant | MODIFIER | c.-836C>T| |
S198 S294 |
| 131353 | BAA10g18610 | A10 | 17382445 | C | T | upstream_gene_variant | MODIFIER | c.-1450G>A| |
S153 S213 |
| 131354 | BAA10g18610 | A10 | 17383032 | C | T | upstream_gene_variant | MODIFIER | c.-2037G>A| |
S25 |
| 131355 | BAA10g18610 | A10 | 17383915 | C | T | upstream_gene_variant | MODIFIER | c.-2920G>A| |
S92 |
| 131356 | BAA10g18610 | A10 | 17384347 | G | A | upstream_gene_variant | MODIFIER | c.-3352C>T| |
S207 |
| 131357 | BAA10g18610 | A10 | 17384579 | C | T | upstream_gene_variant | MODIFIER | c.-3584G>A| |
S259 |
| 131358 | BAA10g18620 | A10 | 17385134 | C | T | synonymous_variant | LOW | c.114C>T|p.Asp38Asp |
S150 |
| 131359 | BAA10g18620 | A10 | 17385356 | C | T | synonymous_variant | LOW | c.336C>T|p.Val112Val |
S168 |
| 131360 | BAA10g18620 | A10 | 17385431 | C | T | synonymous_variant | LOW | c.411C>T|p.Phe137Phe |
S107 |
| 131361 | BAA10g18620 | A10 | 17387324 | G | A | downstream_gene_variant | MODIFIER | c.*350G>A| |
S69 |
| 131362 | BAA10g18620 | A10 | 17387412 | G | A | downstream_gene_variant | MODIFIER | c.*438G>A| |
S205 |
| 131363 | BAA10g18630 | A10 | 17388276 | G | A | upstream_gene_variant | MODIFIER | c.-499C>T| |
S174 S27 |
| 131364 | BAA10g18630 | A10 | 17391224 | C | G | upstream_gene_variant | MODIFIER | c.-3447G>C| |
S76 |
| 131365 | BAA10g18650 | A10 | 17394636 | G | A | upstream_gene_variant | MODIFIER | c.-3816G>A| |
S9 |
| 131366 | BAA10g18650 | A10 | 17395729 | G | A | upstream_gene_variant | MODIFIER | c.-2723G>A| |
S280 |
| 131367 | BAA10g18650 | A10 | 17396012 | G | A | upstream_gene_variant | MODIFIER | c.-2440G>A| |
S138 |
| 131368 | BAA10g18650 | A10 | 17396095 | C | T | upstream_gene_variant | MODIFIER | c.-2357C>T| |
S81 |
| 131369 | BAA10g18640 | A10 | 17396399 | C | T | missense_variant | MODERATE | c.553G>A|p.Val185Met |
S12 |
| 131370 | BAA10g18640 | A10 | 17396600 | G | A | missense_variant | MODERATE | c.434C>T|p.Thr145Ile |
S148 |
| 131371 | BAA10g18640 | A10 | 17397087 | G | A | synonymous_variant | LOW | c.123C>T|p.Ile41Ile |
S217 S248 |
| 131372 | BAA10g18640 | A10 | 17397142 | G | A | missense_variant | MODERATE | c.68C>T|p.Ser23Phe |
S292 |
| 131373 | BAA10g18640 | A10 | 17397343 | G | A | upstream_gene_variant | MODIFIER | c.-10C>T| |
S138 |
| 131374 | BAA10g18640 | A10 | 17397886 | G | A | upstream_gene_variant | MODIFIER | c.-553C>T| |
S223 |
| 131375 | BAA10g18640 | A10 | 17398153 | C | T | upstream_gene_variant | MODIFIER | c.-820G>A| |
S124 |