| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 135801 | BAA10g21600 | A10 | 18942462 | G | A | synonymous_variant | LOW | c.1584C>T|p.Val528Val |
S163 |
| 135802 | BAA10g21600 | A10 | 18942610 | A | G | missense_variant | MODERATE | c.1436T>C|p.Leu479Pro |
S59 |
| 135803 | BAA10g21600 | A10 | 18943845 | G | A | synonymous_variant | LOW | c.201C>T|p.Tyr67Tyr |
S175 |
| 135804 | BAA10g21600 | A10 | 18943867 | G | A | missense_variant | MODERATE | c.179C>T|p.Ser60Phe |
S143 |
| 135805 | BAA10g21600 | A10 | 18944003 | C | T | missense_variant | MODERATE | c.43G>A|p.Glu15Lys |
S114 |
| 135806 | BAA10g21580 | A10 | 18944226 | G | A | upstream_gene_variant | MODIFIER | c.-4805C>T| |
S35 |
| 135807 | BAA10g21580 | A10 | 18944266 | C | T | upstream_gene_variant | MODIFIER | c.-4845G>A| |
S12 |
| 135808 | BAA10g21580 | A10 | 18944284 | C | T | upstream_gene_variant | MODIFIER | c.-4863G>A| |
S187 |
| 135809 | BAA10g21580 | A10 | 18944289 | G | A | upstream_gene_variant | MODIFIER | c.-4868C>T| |
S283 |
| 135810 | BAA10g21600 | A10 | 18946197 | G | A | upstream_gene_variant | MODIFIER | c.-2152C>T| |
S280 |
| 135811 | BAA10g21600 | A10 | 18946696 | G | A | upstream_gene_variant | MODIFIER | c.-2651C>T| |
S228 |
| 135812 | BAA10g21610 | A10 | 18946855 | G | A | synonymous_variant | LOW | c.1578C>T|p.Ile526Ile |
S82 S92 |
| 135813 | BAA10g21610 | A10 | 18947561 | G | A | missense_variant | MODERATE | c.872C>T|p.Ser291Phe |
S241 |
| 135814 | BAA10g21610 | A10 | 18947743 | G | A | synonymous_variant | LOW | c.690C>T|p.His230His |
S193 |
| 135815 | BAA10g21610 | A10 | 18947870 | G | A | missense_variant | MODERATE | c.563C>T|p.Ser188Phe |
S219 S72 |
| 135816 | BAA10g21610 | A10 | 18948185 | G | A | missense_variant | MODERATE | c.248C>T|p.Thr83Met |
S136 |
| 135817 | BAA10g21600 | A10 | 18948691 | C | T | upstream_gene_variant | MODIFIER | c.-4646G>A| |
S92 |
| 135818 | BAA10g21620 | A10 | 18950115 | G | A | missense_variant | MODERATE | c.2128C>T|p.His710Tyr |
S173 |
| 135819 | BAA10g21620 | A10 | 18950362 | C | T | missense_variant | MODERATE | c.1881G>A|p.Met627Ile |
S42 |
| 135820 | BAA10g21620 | A10 | 18950516 | C | T | missense_variant | MODERATE | c.1727G>A|p.Gly576Glu |
S206 S26 |
| 135821 | BAA10g21620 | A10 | 18951907 | C | T | synonymous_variant | LOW | c.336G>A|p.Arg112Arg |
S266 |
| 135822 | BAA10g21610 | A10 | 18952315 | C | T | upstream_gene_variant | MODIFIER | c.-3883G>A| |
S51 |
| 135823 | BAA10g21610 | A10 | 18952479 | C | T | upstream_gene_variant | MODIFIER | c.-4047G>A| |
S275 |
| 135824 | BAA10g21610 | A10 | 18952852 | C | T | upstream_gene_variant | MODIFIER | c.-4420G>A| |
S249 |
| 135825 | BAA10g21610 | A10 | 18952879 | C | T | upstream_gene_variant | MODIFIER | c.-4447G>A| |
S282 |