| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 186851 | BAA02g23960 | A02 | 13092299 | G | A | upstream_gene_variant | MODIFIER | c.-716G>A| |
S67 |
| 186852 | BAA02g23960 | A02 | 13092478 | G | A | upstream_gene_variant | MODIFIER | c.-537G>A| |
S187 |
| 186853 | BAA02g23960 | A02 | 13093148 | C | T | missense_variant | MODERATE | c.134C>T|p.Ser45Phe |
S308 |
| 186854 | BAA02g23960 | A02 | 13093188 | C | T | downstream_gene_variant | MODIFIER | c.*9C>T| |
S212 |
| 186855 | BAA02g23970 | A02 | 13093495 | G | A | missense_variant | MODERATE | c.167C>T|p.Ser56Phe |
S13 |
| 186856 | BAA02g23980 | A02 | 13094753 | C | T | missense_variant | MODERATE | c.2671G>A|p.Glu891Lys |
S8 |
| 186857 | BAA02g23980 | A02 | 13094901 | G | A | synonymous_variant | LOW | c.2523C>T|p.Leu841Leu |
S278 |
| 186858 | BAA02g23980 | A02 | 13096359 | G | A | synonymous_variant | LOW | c.1065C>T|p.Leu355Leu |
S235 |
| 186859 | BAA02g23970 | A02 | 13098599 | T | G | upstream_gene_variant | MODIFIER | c.-4938A>C| |
S82 |
| 186860 | BAA02g23980 | A02 | 13098797 | C | T | upstream_gene_variant | MODIFIER | c.-672G>A| |
S233 |
| 186861 | BAA02g23980 | A02 | 13099693 | G | A | upstream_gene_variant | MODIFIER | c.-1568C>T| |
S249 |
| 186862 | BAA02g23980 | A02 | 13099705 | C | T | upstream_gene_variant | MODIFIER | c.-1580G>A| |
S283 |
| 186863 | BAA02g23980 | A02 | 13099764 | C | T | upstream_gene_variant | MODIFIER | c.-1639G>A| |
S162 |
| 186864 | BAA02g23990 | A02 | 13100181 | C | T | missense_variant | MODERATE | c.1949G>A|p.Gly650Glu |
S144 S203 |
| 186865 | BAA02g23990 | A02 | 13100534 | G | A | synonymous_variant | LOW | c.1596C>T|p.Thr532Thr |
S187 |
| 186866 | BAA02g23990 | A02 | 13100594 | G | A | synonymous_variant | LOW | c.1536C>T|p.Cys512Cys |
S5 |
| 186867 | BAA02g23990 | A02 | 13101116 | C | T | synonymous_variant | LOW | c.1014G>A|p.Gln338Gln |
S115 |
| 186868 | BAA02g23980 | A02 | 13102558 | C | T | upstream_gene_variant | MODIFIER | c.-4433G>A| |
S216 |
| 186869 | BAA02g23990 | A02 | 13103559 | G | A | upstream_gene_variant | MODIFIER | c.-1094C>T| |
S191 |
| 186870 | BAA02g23990 | A02 | 13104123 | C | T | upstream_gene_variant | MODIFIER | c.-1658G>A| |
S138 |
| 186871 | BAA02g23990 | A02 | 13104257 | G | A | upstream_gene_variant | MODIFIER | c.-1792C>T| |
S166 |
| 186872 | BAA02g23990 | A02 | 13106500 | C | T | upstream_gene_variant | MODIFIER | c.-4035G>A| |
S130 |
| 186873 | BAA02g24010 | A02 | 13107116 | C | T | synonymous_variant | LOW | c.1899G>A|p.Leu633Leu |
S41 |
| 186874 | BAA02g24010 | A02 | 13107549 | G | A | missense_variant | MODERATE | c.1466C>T|p.Thr489Met |
S247 |
| 186875 | BAA02g24010 | A02 | 13107661 | G | A | missense_variant | MODERATE | c.1354C>T|p.Pro452Ser |
S25 |