| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g30560 | A01 | 19528785 | C | T | downstream_gene_variant | MODIFIER | c.*4153G>A| |
S150 |
| 2 | BAA01g30560 | A01 | 19532213 | C | T | downstream_gene_variant | MODIFIER | c.*725G>A| |
S166 |
| 3 | BAA01g30560 | A01 | 19534205 | G | A | missense_variant | MODERATE | c.1121C>T|p.Ser374Leu |
S174 S27 |
| 4 | BAA01g30560 | A01 | 19534364 | G | A | intron_variant | MODIFIER | c.1118-156C>T| |
S62 |
| 5 | BAA01g30560 | A01 | 19534558 | C | T | intron_variant | MODIFIER | c.1118-350G>A| |
S205 |
| 6 | BAA01g30560 | A01 | 19536050 | G | A | missense_variant | MODERATE | c.845C>T|p.Pro282Leu |
S274 |
| 7 | BAA01g30560 | A01 | 19536394 | C | T | splice_region_variant&intron_variant | LOW | c.642+5G>A| |
S50 |
| 8 | BAA01g30560 | A01 | 19537036 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.445-1G>A| |
S41 |
| 9 | BAA01g30560 | A01 | 19537798 | C | T | intron_variant | MODIFIER | c.195+53G>A| |
S69 |
| 10 | BAA01g30560 | A01 | 19537812 | G | A | intron_variant | MODIFIER | c.195+39C>T| |
S299 |
| 11 | BAA01g30560 | A01 | 19538349 | C | T | upstream_gene_variant | MODIFIER | c.-129G>A| |
S200 |
| 12 | BAA01g30560 | A01 | 19540647 | G | A | upstream_gene_variant | MODIFIER | c.-2427C>T| |
S199 |
| 13 | BAA01g30560 | A01 | 19541181 | C | T | upstream_gene_variant | MODIFIER | c.-2961G>A| |
S19 |
| 14 | BAA01g30560 | A01 | 19541273 | C | A | upstream_gene_variant | MODIFIER | c.-3053G>T| |
S122 |
| 15 | BAA01g30560 | A01 | 19541449 | G | A | upstream_gene_variant | MODIFIER | c.-3229C>T| |
S199 |
| 16 | BAA01g30560 | A01 | 19541851 | C | T | upstream_gene_variant | MODIFIER | c.-3631G>A| |
S162 |