| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 150051 | BAA10g34110 | A10 | 24082519 | C | T | missense_variant | MODERATE | c.1868C>T|p.Thr623Ile |
S148 S210 S30 S31 |
| 150052 | BAA10g34100 | A10 | 24083714 | C | T | upstream_gene_variant | MODIFIER | c.-4338G>A| |
S209 |
| 150053 | BAA10g34120 | A10 | 24083965 | C | T | missense_variant | MODERATE | c.1168G>A|p.Glu390Lys |
S94 |
| 150054 | BAA10g34120 | A10 | 24084364 | C | T | missense_variant | MODERATE | c.769G>A|p.Val257Ile |
S87 |
| 150055 | BAA10g34120 | A10 | 24084453 | C | T | missense_variant | MODERATE | c.680G>A|p.Cys227Tyr |
S200 |
| 150056 | BAA10g34130 | A10 | 24086114 | G | A | missense_variant | MODERATE | c.85G>A|p.Val29Ile |
S219 S72 |
| 150057 | BAA10g34120 | A10 | 24086163 | G | A | upstream_gene_variant | MODIFIER | c.-887C>T| |
S303 |
| 150058 | BAA10g34130 | A10 | 24086584 | G | A | stop_gained | HIGH | c.305G>A|p.Trp102* |
S197 |
| 150059 | BAA10g34130 | A10 | 24086677 | G | A | missense_variant | MODERATE | c.398G>A|p.Cys133Tyr |
S100 |
| 150060 | BAA10g34130 | A10 | 24086843 | G | A | missense_variant | MODERATE | c.487G>A|p.Glu163Lys |
S100 |
| 150061 | BAA10g34130 | A10 | 24087157 | G | A | splice_region_variant&intron_variant | LOW | c.705+5G>A| |
S182 |
| 150062 | BAA10g34130 | A10 | 24087754 | G | A | splice_region_variant&intron_variant | LOW | c.1048+6G>A| |
S280 |
| 150063 | BAA10g34130 | A10 | 24087952 | G | A | missense_variant | MODERATE | c.1151G>A|p.Gly384Glu |
S174 S27 |
| 150064 | BAA10g34130 | A10 | 24088406 | G | A | missense_variant | MODERATE | c.1528G>A|p.Glu510Lys |
S200 |
| 150065 | BAA10g34130 | A10 | 24089216 | G | A | missense_variant | MODERATE | c.2158G>A|p.Gly720Ser |
S299 |
| 150066 | BAA10g34120 | A10 | 24089612 | G | A | upstream_gene_variant | MODIFIER | c.-4336C>T| |
S68 |
| 150067 | BAA10g34120 | A10 | 24090166 | G | A | upstream_gene_variant | MODIFIER | c.-4890C>T| |
|
| 150068 | BAA10g34140 | A10 | 24090680 | G | A | upstream_gene_variant | MODIFIER | c.-3208G>A| |
S74 |
| 150069 | BAA10g34140 | A10 | 24091413 | G | A | upstream_gene_variant | MODIFIER | c.-2475G>A| |
S99 |
| 150070 | BAA10g34140 | A10 | 24092123 | G | A | upstream_gene_variant | MODIFIER | c.-1765G>A| |
S263 |
| 150071 | BAA10g34140 | A10 | 24092692 | C | T | upstream_gene_variant | MODIFIER | c.-1196C>T| |
S229 |
| 150072 | BAA10g34140 | A10 | 24092877 | G | A | upstream_gene_variant | MODIFIER | c.-1011G>A| |
S128 |
| 150073 | BAA10g34140 | A10 | 24093354 | C | T | upstream_gene_variant | MODIFIER | c.-534C>T| |
S20 |
| 150074 | BAA10g34140 | A10 | 24093982 | C | T | missense_variant | MODERATE | c.95C>T|p.Ser32Leu |
S246 |
| 150075 | BAA10g34140 | A10 | 24094693 | G | A | missense_variant | MODERATE | c.806G>A|p.Arg269Gln |
S59 |