| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 184901 | BAA02g22830 | A02 | 12371948 | C | T | downstream_gene_variant | MODIFIER | c.*759C>T| |
S305 |
| 184902 | BAA02g22830 | A02 | 12372146 | C | T | downstream_gene_variant | MODIFIER | c.*957C>T| |
S183 S198 |
| 184903 | BAA02g22830 | A02 | 12372359 | G | A | downstream_gene_variant | MODIFIER | c.*1170G>A| |
S109 |
| 184904 | BAA02g22830 | A02 | 12372720 | C | T | downstream_gene_variant | MODIFIER | c.*1531C>T| |
S142 |
| 184905 | BAA02g22830 | A02 | 12374505 | G | A | downstream_gene_variant | MODIFIER | c.*3316G>A| |
S25 |
| 184906 | BAA02g22850 | A02 | 12381192 | G | A | upstream_gene_variant | MODIFIER | c.-2522G>A| |
S187 |
| 184907 | BAA02g22850 | A02 | 12382991 | C | T | upstream_gene_variant | MODIFIER | c.-723C>T| |
S157 S163 |
| 184908 | BAA02g22840 | A02 | 12384899 | C | T | upstream_gene_variant | MODIFIER | c.-1251G>A| |
S241 |
| 184909 | BAA02g22840 | A02 | 12385042 | C | T | upstream_gene_variant | MODIFIER | c.-1394G>A| |
S2 |
| 184910 | BAA02g22840 | A02 | 12385891 | C | T | upstream_gene_variant | MODIFIER | c.-2243G>A| |
S283 |
| 184911 | BAA02g22840 | A02 | 12388334 | G | A | upstream_gene_variant | MODIFIER | c.-4686C>T| |
S281 |
| 184912 | BAA02g22840 | A02 | 12388545 | G | A | upstream_gene_variant | MODIFIER | c.-4897C>T| |
S251 |
| 184913 | BAA02g22850 | A02 | 12388889 | C | T | intron_variant | MODIFIER | c.43-1758C>T| |
S140 |
| 184914 | BAA02g22850 | A02 | 12388994 | C | T | intron_variant | MODIFIER | c.43-1653C>T| |
S123 |
| 184915 | BAA02g22850 | A02 | 12389370 | G | A | intron_variant | MODIFIER | c.43-1277G>A| |
S111 |
| 184916 | BAA02g22850 | A02 | 12390427 | G | A | intron_variant | MODIFIER | c.43-220G>A| |
S232 |
| 184917 | BAA02g22850 | A02 | 12390672 | G | A | missense_variant | MODERATE | c.68G>A|p.Ser23Asn |
S132 S137 S215 |
| 184918 | BAA02g22850 | A02 | 12390741 | C | T | missense_variant | MODERATE | c.137C>T|p.Pro46Leu |
S207 |
| 184919 | BAA02g22850 | A02 | 12391040 | C | T | missense_variant | MODERATE | c.436C>T|p.Arg146Trp |
S221 |
| 184920 | BAA02g22850 | A02 | 12391109 | G | A | missense_variant | MODERATE | c.505G>A|p.Glu169Lys |
S28 |
| 184921 | BAA02g22850 | A02 | 12391186 | G | A | synonymous_variant | LOW | c.582G>A|p.Val194Val |
S263 |
| 184922 | BAA02g22850 | A02 | 12391299 | G | A | missense_variant | MODERATE | c.695G>A|p.Arg232Gln |
S166 |
| 184923 | BAA02g22850 | A02 | 12391724 | C | T | downstream_gene_variant | MODIFIER | c.*394C>T| |
S73 S91 |
| 184924 | BAA02g22850 | A02 | 12392287 | G | A | downstream_gene_variant | MODIFIER | c.*957G>A| |
S90 |
| 184925 | BAA02g22850 | A02 | 12392636 | G | A | downstream_gene_variant | MODIFIER | c.*1306G>A| |
S294 |