| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 70851 | BAA01g37170 | A01 | 24807856 | G | A | upstream_gene_variant | MODIFIER | c.-885C>T| |
S172 |
| 70852 | BAA01g37180 | A01 | 24808038 | G | A | missense_variant | MODERATE | c.104G>A|p.Gly35Glu |
S74 |
| 70853 | BAA01g37180 | A01 | 24808256 | G | A | missense_variant | MODERATE | c.322G>A|p.Glu108Lys |
S100 |
| 70854 | BAA01g37180 | A01 | 24808340 | G | A | missense_variant | MODERATE | c.406G>A|p.Glu136Lys |
S181 |
| 70855 | BAA01g37180 | A01 | 24808543 | G | T | missense_variant | MODERATE | c.609G>T|p.Arg203Ser |
S278 |
| 70856 | BAA01g37180 | A01 | 24808595 | C | T | missense_variant | MODERATE | c.661C>T|p.Arg221Cys |
S181 |
| 70857 | BAA01g37180 | A01 | 24808768 | G | A | synonymous_variant | LOW | c.834G>A|p.Arg278Arg |
S299 |
| 70858 | BAA01g37180 | A01 | 24809313 | C | T | missense_variant | MODERATE | c.1301C>T|p.Ala434Val |
S211 S227 |
| 70859 | BAA01g37180 | A01 | 24809588 | C | T | synonymous_variant | LOW | c.1576C>T|p.Leu526Leu |
S16 S181 S56 |
| 70860 | BAA01g37180 | A01 | 24809960 | C | T | missense_variant | MODERATE | c.1948C>T|p.Pro650Ser |
S133 |
| 70861 | BAA01g37170 | A01 | 24811159 | C | T | upstream_gene_variant | MODIFIER | c.-4188G>A| |
S94 |
| 70862 | BAA01g37170 | A01 | 24811218 | C | T | upstream_gene_variant | MODIFIER | c.-4247G>A| |
S264 |
| 70863 | BAA01g37190 | A01 | 24812172 | C | T | upstream_gene_variant | MODIFIER | c.-1376C>T| |
S92 |
| 70864 | BAA01g37190 | A01 | 24813371 | G | A | upstream_gene_variant | MODIFIER | c.-177G>A| |
S294 |
| 70865 | BAA01g37190 | A01 | 24813553 | G | A | missense_variant | MODERATE | c.6G>A|p.Met2Ile |
S259 |
| 70866 | BAA01g37190 | A01 | 24814576 | C | T | missense_variant | MODERATE | c.775C>T|p.Pro259Ser |
S301 S304 |
| 70867 | BAA01g37190 | A01 | 24815469 | C | T | missense_variant | MODERATE | c.953C>T|p.Ala318Val |
S255 |
| 70868 | BAA01g37190 | A01 | 24816115 | C | T | missense_variant | MODERATE | c.1324C>T|p.Pro442Ser |
S239 |
| 70869 | BAA01g37190 | A01 | 24816481 | G | A | missense_variant | MODERATE | c.1528G>A|p.Ala510Thr |
S176 |
| 70870 | BAA01g37190 | A01 | 24817253 | C | T | splice_region_variant&intron_variant | LOW | c.2042-8C>T| |
S72 S78 |
| 70871 | BAA01g37190 | A01 | 24817903 | C | T | synonymous_variant | LOW | c.2448C>T|p.Leu816Leu |
S272 |
| 70872 | BAA01g37200 | A01 | 24818719 | G | A | upstream_gene_variant | MODIFIER | c.-371G>A| |
S252 |
| 70873 | BAA01g37200 | A01 | 24819287 | C | T | synonymous_variant | LOW | c.198C>T|p.Ser66Ser |
S142 |
| 70874 | BAA01g37210 | A01 | 24820736 | G | A | synonymous_variant | LOW | c.558G>A|p.Glu186Glu |
S14 |
| 70875 | BAA01g37210 | A01 | 24821063 | G | A | synonymous_variant | LOW | c.885G>A|p.Gln295Gln |
S223 |