| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 157851 | BAA02g05510 | A02 | 2385467 | C | T | missense_variant | MODERATE | c.308G>A|p.Gly103Glu |
S267 |
| 157852 | BAA02g05490 | A02 | 2385627 | G | A | downstream_gene_variant | MODIFIER | c.*3719G>A| |
S263 |
| 157853 | BAA02g05490 | A02 | 2385699 | G | A | downstream_gene_variant | MODIFIER | c.*3791G>A| |
S283 |
| 157854 | BAA02g05490 | A02 | 2385855 | G | A | downstream_gene_variant | MODIFIER | c.*3947G>A| |
S13 S168 S219 S279 S64 |
| 157855 | BAA02g05490 | A02 | 2385969 | G | A | downstream_gene_variant | MODIFIER | c.*4061G>A| |
S283 |
| 157856 | BAA02g05510 | A02 | 2387017 | G | A | upstream_gene_variant | MODIFIER | c.-569C>T| |
S197 |
| 157857 | BAA02g05510 | A02 | 2388607 | G | A | upstream_gene_variant | MODIFIER | c.-2159C>T| |
S177 |
| 157858 | BAA02g05510 | A02 | 2388662 | G | A | upstream_gene_variant | MODIFIER | c.-2214C>T| |
S303 |
| 157859 | BAA02g05520 | A02 | 2388957 | G | A | missense_variant | MODERATE | c.311C>T|p.Ser104Leu |
S235 |
| 157860 | BAA02g05520 | A02 | 2389128 | C | T | missense_variant | MODERATE | c.140G>A|p.Gly47Glu |
S18 |
| 157861 | BAA02g05510 | A02 | 2390013 | C | T | upstream_gene_variant | MODIFIER | c.-3565G>A| |
S8 |
| 157862 | BAA02g05510 | A02 | 2390044 | C | T | upstream_gene_variant | MODIFIER | c.-3596G>A| |
S159 S187 S188 S243 S276 S299 |
| 157863 | BAA02g05510 | A02 | 2390220 | C | T | upstream_gene_variant | MODIFIER | c.-3772G>A| |
S202 |
| 157864 | BAA02g05510 | A02 | 2390256 | C | T | upstream_gene_variant | MODIFIER | c.-3808G>A| |
S13 |
| 157865 | BAA02g05520 | A02 | 2392178 | G | A | upstream_gene_variant | MODIFIER | c.-2831C>T| |
S291 |
| 157866 | BAA02g05520 | A02 | 2392810 | G | A | upstream_gene_variant | MODIFIER | c.-3463C>T| |
S143 |
| 157867 | BAA02g05530 | A02 | 2393595 | G | A | missense_variant | MODERATE | c.79G>A|p.Val27Ile |
S109 |
| 157868 | BAA02g05530 | A02 | 2394249 | C | T | synonymous_variant | LOW | c.652C>T|p.Leu218Leu |
S185 |
| 157869 | BAA02g05530 | A02 | 2395189 | G | A | missense_variant | MODERATE | c.1322G>A|p.Arg441His |
S223 |
| 157870 | BAA02g05530 | A02 | 2396344 | G | A | downstream_gene_variant | MODIFIER | c.*690G>A| |
S149 |
| 157871 | BAA02g05530 | A02 | 2396692 | C | T | downstream_gene_variant | MODIFIER | c.*1038C>T| |
S178 |
| 157872 | BAA02g05540 | A02 | 2396939 | C | T | synonymous_variant | LOW | c.327G>A|p.Gln109Gln |
S58 |
| 157873 | BAA02g05530 | A02 | 2397050 | G | A | downstream_gene_variant | MODIFIER | c.*1396G>A| |
S232 |
| 157874 | BAA02g05540 | A02 | 2397882 | C | T | upstream_gene_variant | MODIFIER | c.-136G>A| |
S142 |
| 157875 | BAA02g05540 | A02 | 2397991 | C | T | upstream_gene_variant | MODIFIER | c.-245G>A| |
S46 |