| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA04g12630 | A04 | 18320095 | G | A | downstream_gene_variant | MODIFIER | c.*4668C>T| |
S12 |
| 2 | BAA04g12630 | A04 | 18320132 | C | T | downstream_gene_variant | MODIFIER | c.*4631G>A| |
S260 |
| 3 | BAA04g12630 | A04 | 18320431 | G | A | downstream_gene_variant | MODIFIER | c.*4332C>T| |
S138 |
| 4 | BAA04g12630 | A04 | 18320525 | C | T | downstream_gene_variant | MODIFIER | c.*4238G>A| |
S302 |
| 5 | BAA04g12630 | A04 | 18321053 | G | A | downstream_gene_variant | MODIFIER | c.*3710C>T| |
S95 |
| 6 | BAA04g12630 | A04 | 18321095 | C | T | downstream_gene_variant | MODIFIER | c.*3668G>A| |
S263 |
| 7 | BAA04g12630 | A04 | 18321298 | G | A | downstream_gene_variant | MODIFIER | c.*3465C>T| |
S164 |
| 8 | BAA04g12630 | A04 | 18321535 | C | T | downstream_gene_variant | MODIFIER | c.*3228G>A| |
S280 |
| 9 | BAA04g12630 | A04 | 18322536 | G | A | downstream_gene_variant | MODIFIER | c.*2227C>T| |
S165 |
| 10 | BAA04g12630 | A04 | 18324502 | G | A | downstream_gene_variant | MODIFIER | c.*261C>T| |
S70 |
| 11 | BAA04g12630 | A04 | 18324653 | G | A | downstream_gene_variant | MODIFIER | c.*110C>T| |
S238 |
| 12 | BAA04g12630 | A04 | 18324675 | C | T | downstream_gene_variant | MODIFIER | c.*88G>A| |
S267 |
| 13 | BAA04g12630 | A04 | 18324768 | C | T | missense_variant | MODERATE | c.1459G>A|p.Glu487Lys |
S140 |
| 14 | BAA04g12630 | A04 | 18324842 | G | A | missense_variant | MODERATE | c.1385C>T|p.Ala462Val |
S171 |
| 15 | BAA04g12630 | A04 | 18324863 | G | C | missense_variant | MODERATE | c.1364C>G|p.Thr455Arg |
S218 |
| 16 | BAA04g12630 | A04 | 18325455 | G | A | intron_variant | MODIFIER | c.966-36C>T| |
S19 |
| 17 | BAA04g12630 | A04 | 18326331 | C | T | intron_variant | MODIFIER | c.510-16G>A| |
S257 |
| 18 | BAA04g12630 | A04 | 18326439 | G | A | stop_gained | HIGH | c.457C>T|p.Gln153* |
S303 |
| 19 | BAA04g12630 | A04 | 18326495 | G | A | intron_variant | MODIFIER | c.413-12C>T| |
S239 |
| 20 | BAA04g12630 | A04 | 18326957 | C | T | missense_variant | MODERATE | c.110G>A|p.Gly37Asp |
S2 |
| 21 | BAA04g12630 | A04 | 18327120 | C | T | upstream_gene_variant | MODIFIER | c.-54G>A| |
S295 |
| 22 | BAA04g12630 | A04 | 18328719 | G | A | upstream_gene_variant | MODIFIER | c.-1653C>T| |
S166 |
| 23 | BAA04g12630 | A04 | 18329102 | C | T | upstream_gene_variant | MODIFIER | c.-2036G>A| |
S225 S73 |
| 24 | BAA04g12630 | A04 | 18329357 | G | A | upstream_gene_variant | MODIFIER | c.-2291C>T| |
S162 |
| 25 | BAA04g12630 | A04 | 18329856 | G | A | upstream_gene_variant | MODIFIER | c.-2790C>T| |
S40 S49 S86 |