| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 130401 | BAA10g17990 | A10 | 17064814 | G | A | upstream_gene_variant | MODIFIER | c.-3862C>T| |
S287 |
| 130402 | BAA10g17990 | A10 | 17064893 | G | A | upstream_gene_variant | MODIFIER | c.-3941C>T| |
S67 |
| 130403 | BAA10g17990 | A10 | 17065054 | G | A | upstream_gene_variant | MODIFIER | c.-4102C>T| |
S288 |
| 130404 | BAA10g17990-BAA10g18000 | A10 | 17066745 | C | T | intergenic_region | MODIFIER | n.17066745C>T| |
S152 |
| 130405 | BAA10g18000 | A10 | 17068194 | G | A | upstream_gene_variant | MODIFIER | c.-4456G>A| |
S283 |
| 130406 | BAA10g18000 | A10 | 17068264 | C | T | upstream_gene_variant | MODIFIER | c.-4386C>T| |
S162 |
| 130407 | BAA10g18000 | A10 | 17068328 | C | T | upstream_gene_variant | MODIFIER | c.-4322C>T| |
S37 |
| 130408 | BAA10g18000 | A10 | 17069979 | C | T | upstream_gene_variant | MODIFIER | c.-2671C>T| |
S2 |
| 130409 | BAA10g18000 | A10 | 17070882 | C | T | upstream_gene_variant | MODIFIER | c.-1768C>T| |
S68 |
| 130410 | BAA10g18000 | A10 | 17071455 | C | T | upstream_gene_variant | MODIFIER | c.-1195C>T| |
S47 |
| 130411 | BAA10g18000 | A10 | 17071576 | G | A | upstream_gene_variant | MODIFIER | c.-1074G>A| |
S234 |
| 130412 | BAA10g18000 | A10 | 17071725 | C | T | upstream_gene_variant | MODIFIER | c.-925C>T| |
S44 |
| 130413 | BAA10g18000 | A10 | 17072388 | G | A | upstream_gene_variant | MODIFIER | c.-262G>A| |
S94 |
| 130414 | BAA10g18000 | A10 | 17073042 | G | A | stop_gained | HIGH | c.393G>A|p.Trp131* |
S112 |
| 130415 | BAA10g18000 | A10 | 17073258 | G | A | synonymous_variant | LOW | c.609G>A|p.Lys203Lys |
S32 |
| 130416 | BAA10g18000 | A10 | 17073544 | C | T | missense_variant | MODERATE | c.895C>T|p.Leu299Phe |
S187 |
| 130417 | BAA10g18000 | A10 | 17073922 | G | A | missense_variant | MODERATE | c.1273G>A|p.Asp425Asn |
S280 |
| 130418 | BAA10g18000 | A10 | 17073973 | G | A | missense_variant | MODERATE | c.1324G>A|p.Ala442Thr |
S66 |
| 130419 | BAA10g18000 | A10 | 17074304 | G | A | missense_variant | MODERATE | c.1655G>A|p.Gly552Glu |
S261 |
| 130420 | BAA10g18020 | A10 | 17074874 | C | T | upstream_gene_variant | MODIFIER | c.-2499C>T| |
S209 |
| 130421 | BAA10g18020 | A10 | 17075455 | G | A | upstream_gene_variant | MODIFIER | c.-1918G>A| |
S270 |
| 130422 | BAA10g18020 | A10 | 17075573 | G | A | upstream_gene_variant | MODIFIER | c.-1800G>A| |
S212 |
| 130423 | BAA10g18010 | A10 | 17076065 | C | T | missense_variant | MODERATE | c.506G>A|p.Arg169Gln |
S189 |
| 130424 | BAA10g18020 | A10 | 17077502 | G | A | missense_variant | MODERATE | c.130G>A|p.Ala44Thr |
S198 |
| 130425 | BAA10g18030 | A10 | 17080404 | C | T | synonymous_variant | LOW | c.243C>T|p.Phe81Phe |
S230 |