| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 145851 | BAA10g30280 | A10 | 22524864 | G | A | upstream_gene_variant | MODIFIER | c.-3832C>T| |
S199 |
| 145852 | BAA10g30280 | A10 | 22524935 | G | A | upstream_gene_variant | MODIFIER | c.-3903C>T| |
S226 |
| 145853 | BAA10g30280 | A10 | 22525087 | C | T | upstream_gene_variant | MODIFIER | c.-4055G>A| |
S45 |
| 145854 | BAA10g30290 | A10 | 22525416 | C | T | missense_variant | MODERATE | c.239C>T|p.Ala80Val |
S185 |
| 145855 | BAA10g30290 | A10 | 22525427 | C | T | synonymous_variant | LOW | c.250C>T|p.Leu84Leu |
S48 |
| 145856 | BAA10g30290 | A10 | 22525881 | G | A | missense_variant | MODERATE | c.704G>A|p.Gly235Asp |
S7 |
| 145857 | BAA10g30290 | A10 | 22525900 | G | A | synonymous_variant | LOW | c.723G>A|p.Lys241Lys |
S113 |
| 145858 | BAA10g30290 | A10 | 22526009 | G | A | missense_variant | MODERATE | c.832G>A|p.Asp278Asn |
S182 |
| 145859 | BAA10g30290 | A10 | 22526777 | G | A | downstream_gene_variant | MODIFIER | c.*748G>A| |
S158 |
| 145860 | BAA10g30300 | A10 | 22526883 | G | A | missense_variant | MODERATE | c.256G>A|p.Asp86Asn |
S77 |
| 145861 | BAA10g30300 | A10 | 22526916 | G | A | missense_variant | MODERATE | c.289G>A|p.Ala97Thr |
S171 |
| 145862 | BAA10g30300 | A10 | 22527324 | G | A | missense_variant | MODERATE | c.527G>A|p.Arg176Lys |
S35 |
| 145863 | BAA10g30300 | A10 | 22527724 | G | A | missense_variant | MODERATE | c.746G>A|p.Gly249Glu |
S117 |
| 145864 | BAA10g30290 | A10 | 22528635 | C | T | downstream_gene_variant | MODIFIER | c.*2606C>T| |
S224 |
| 145865 | BAA10g30300 | A10 | 22528727 | C | T | missense_variant | MODERATE | c.1313C>T|p.Ser438Phe |
S152 |
| 145866 | BAA10g30300 | A10 | 22529252 | C | T | synonymous_variant | LOW | c.1674C>T|p.Pro558Pro |
S242 |
| 145867 | BAA10g30310 | A10 | 22530948 | G | A | synonymous_variant | LOW | c.1923C>T|p.Ile641Ile |
S159 S243 |
| 145868 | BAA10g30310 | A10 | 22531517 | G | A | synonymous_variant | LOW | c.1600C>T|p.Leu534Leu |
S77 |
| 145869 | BAA10g30310 | A10 | 22532052 | C | T | missense_variant | MODERATE | c.1141G>A|p.Ala381Thr |
S275 |
| 145870 | BAA10g30320 | A10 | 22532446 | C | T | upstream_gene_variant | MODIFIER | c.-2377C>T| |
S195 |
| 145871 | BAA10g30310 | A10 | 22533657 | C | T | synonymous_variant | LOW | c.72G>A|p.Gln24Gln |
S281 |
| 145872 | BAA10g30320 | A10 | 22535155 | G | A | missense_variant | MODERATE | c.241G>A|p.Asp81Asn |
S136 |
| 145873 | BAA10g30320 | A10 | 22535235 | C | T | synonymous_variant | LOW | c.321C>T|p.Val107Val |
S36 |
| 145874 | BAA10g30320 | A10 | 22535623 | C | T | synonymous_variant | LOW | c.615C>T|p.Asn205Asn |
S112 |
| 145875 | BAA10g30310 | A10 | 22536079 | G | A | upstream_gene_variant | MODIFIER | c.-2351C>T| |
S288 |