| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 91851 | BAA10g01780 | A10 | 851490 | C | T | upstream_gene_variant | MODIFIER | c.-986G>A| |
S163 |
| 91852 | BAA10g01790 | A10 | 852585 | G | A | missense_variant | MODERATE | c.166G>A|p.Glu56Lys |
S85 |
| 91853 | BAA10g01790 | A10 | 852823 | G | A | stop_gained | HIGH | c.404G>A|p.Trp135* |
S157 S163 |
| 91854 | BAA10g01790 | A10 | 852864 | G | A | missense_variant | MODERATE | c.445G>A|p.Asp149Asn |
S19 |
| 91855 | BAA10g01790 | A10 | 854280 | C | T | missense_variant | MODERATE | c.1405C>T|p.Leu469Phe |
S265 |
| 91856 | BAA10g01790 | A10 | 854350 | G | A | missense_variant | MODERATE | c.1475G>A|p.Gly492Glu |
S261 |
| 91857 | BAA10g01780 | A10 | 855489 | C | T | upstream_gene_variant | MODIFIER | c.-4985G>A| |
S188 |
| 91858 | BAA10g01790 | A10 | 855537 | G | A | downstream_gene_variant | MODIFIER | c.*804G>A| |
S19 |
| 91859 | BAA10g01800 | A10 | 858844 | G | A | missense_variant | MODERATE | c.8132C>T|p.Ser2711Phe |
S168 |
| 91860 | BAA10g01800 | A10 | 859222 | C | T | missense_variant | MODERATE | c.7754G>A|p.Arg2585His |
S244 |
| 91861 | BAA10g01800 | A10 | 859235 | G | A | missense_variant | MODERATE | c.7741C>T|p.Leu2581Phe |
S295 |
| 91862 | BAA10g01800 | A10 | 859619 | C | T | missense_variant | MODERATE | c.7357G>A|p.Val2453Ile |
S241 S39 |
| 91863 | BAA10g01800 | A10 | 859632 | G | A | synonymous_variant | LOW | c.7344C>T|p.Asn2448Asn |
S64 |
| 91864 | BAA10g01800 | A10 | 859759 | C | T | missense_variant | MODERATE | c.7217G>A|p.Cys2406Tyr |
S122 |
| 91865 | BAA10g01800 | A10 | 860093 | C | T | missense_variant | MODERATE | c.6883G>A|p.Asp2295Asn |
S275 |
| 91866 | BAA10g01800 | A10 | 860557 | G | A | missense_variant | MODERATE | c.6419C>T|p.Ser2140Leu |
S107 |
| 91867 | BAA10g01800 | A10 | 861185 | C | T | intron_variant | MODIFIER | c.5817-26G>A| |
S287 |
| 91868 | BAA10g01800 | A10 | 861345 | G | A | missense_variant | MODERATE | c.5797C>T|p.Leu1933Phe |
S219 |
| 91869 | BAA10g01800 | A10 | 862227 | G | A | missense_variant | MODERATE | c.4915C>T|p.Pro1639Ser |
S230 |
| 91870 | BAA10g01800 | A10 | 862853 | G | A | missense_variant | MODERATE | c.4289C>T|p.Ser1430Phe |
S76 |
| 91871 | BAA10g01800 | A10 | 863035 | C | T | intron_variant | MODIFIER | c.4165+36G>A| |
S114 |
| 91872 | BAA10g01800 | A10 | 863085 | G | A | missense_variant | MODERATE | c.4151C>T|p.Ala1384Val |
S251 |
| 91873 | BAA10g01800 | A10 | 863117 | G | A | synonymous_variant | LOW | c.4119C>T|p.Leu1373Leu |
S148 S210 S30 |
| 91874 | BAA10g01800 | A10 | 863179 | G | A | missense_variant | MODERATE | c.4057C>T|p.Leu1353Phe |
S83 S88 |
| 91875 | BAA10g01800 | A10 | 863260 | C | T | missense_variant | MODERATE | c.3976G>A|p.Asp1326Asn |
S270 |