| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 132801 | BAA10g19540 | A10 | 17897150 | C | T | upstream_gene_variant | MODIFIER | c.-194G>A| |
S196 |
| 132802 | BAA10g19550 | A10 | 17897712 | G | A | missense_variant | MODERATE | c.1195C>T|p.Leu399Phe |
S43 |
| 132803 | BAA10g19540 | A10 | 17898848 | G | A | upstream_gene_variant | MODIFIER | c.-1892C>T| |
S202 |
| 132804 | BAA10g19540 | A10 | 17899038 | G | A | upstream_gene_variant | MODIFIER | c.-2082C>T| |
S67 |
| 132805 | BAA10g19540 | A10 | 17899241 | C | T | upstream_gene_variant | MODIFIER | c.-2285G>A| |
S247 |
| 132806 | BAA10g19550 | A10 | 17899339 | C | T | missense_variant | MODERATE | c.524G>A|p.Gly175Glu |
S72 |
| 132807 | BAA10g19540 | A10 | 17900865 | G | A | upstream_gene_variant | MODIFIER | c.-3909C>T| |
S184 |
| 132808 | BAA10g19550 | A10 | 17903146 | C | T | upstream_gene_variant | MODIFIER | c.-2611G>A| |
S38 |
| 132809 | BAA10g19570 | A10 | 17903594 | G | A | missense_variant | MODERATE | c.2365C>T|p.Pro789Ser |
S202 |
| 132810 | BAA10g19570 | A10 | 17904177 | C | T | synonymous_variant | LOW | c.1782G>A|p.Glu594Glu |
S269 |
| 132811 | BAA10g19570 | A10 | 17904179 | C | T | missense_variant | MODERATE | c.1780G>A|p.Glu594Lys |
S195 |
| 132812 | BAA10g19570 | A10 | 17904819 | G | A | synonymous_variant | LOW | c.1140C>T|p.Val380Val |
S240 |
| 132813 | BAA10g19560 | A10 | 17905570 | G | A | downstream_gene_variant | MODIFIER | c.*2704G>A| |
S164 |
| 132814 | BAA10g19570 | A10 | 17905990 | C | T | missense_variant | MODERATE | c.748G>A|p.Asp250Asn |
S2 |
| 132815 | BAA10g19570 | A10 | 17906012 | C | T | synonymous_variant | LOW | c.726G>A|p.Lys242Lys |
S47 |
| 132816 | BAA10g19570 | A10 | 17906583 | G | A | synonymous_variant | LOW | c.483C>T|p.Ser161Ser |
S118 |
| 132817 | BAA10g19570 | A10 | 17906756 | C | T | splice_donor_variant&intron_variant | HIGH | c.414+1G>A| |
S169 |
| 132818 | BAA10g19570 | A10 | 17907084 | G | A | splice_region_variant&intron_variant | LOW | c.235-4C>T| |
S289 S290 |
| 132819 | BAA10g19570 | A10 | 17908339 | G | A | upstream_gene_variant | MODIFIER | c.-788C>T| |
S240 |
| 132820 | BAA10g19580 | A10 | 17909278 | C | T | missense_variant | MODERATE | c.275G>A|p.Arg92Lys |
S246 |
| 132821 | BAA10g19580 | A10 | 17909315 | G | A | missense_variant | MODERATE | c.238C>T|p.Pro80Ser |
S175 |
| 132822 | BAA10g19570 | A10 | 17910245 | G | A | upstream_gene_variant | MODIFIER | c.-2694C>T| |
S184 |
| 132823 | BAA10g19570 | A10 | 17910817 | G | A | upstream_gene_variant | MODIFIER | c.-3266C>T| |
S273 |
| 132824 | BAA10g19570 | A10 | 17910844 | G | A | upstream_gene_variant | MODIFIER | c.-3293C>T| |
S278 |
| 132825 | BAA10g19570 | A10 | 17910894 | G | A | upstream_gene_variant | MODIFIER | c.-3343C>T| |
S228 |