| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA04g17980 | A04 | 22042039 | C | T | downstream_gene_variant | MODIFIER | c.*3472G>A| |
S308 |
| 2 | BAA04g17980 | A04 | 22042111 | G | A | downstream_gene_variant | MODIFIER | c.*3400C>T| |
S114 |
| 3 | BAA04g17980 | A04 | 22043378 | C | T | downstream_gene_variant | MODIFIER | c.*2133G>A| |
S80 |
| 4 | BAA04g17980 | A04 | 22044422 | C | T | downstream_gene_variant | MODIFIER | c.*1089G>A| |
S67 |
| 5 | BAA04g17980 | A04 | 22045823 | C | T | splice_region_variant&intron_variant | LOW | c.1261-4G>A| |
S76 |
| 6 | BAA04g17980 | A04 | 22046185 | C | T | synonymous_variant | LOW | c.978G>A|p.Thr326Thr |
S65 |
| 7 | BAA04g17980 | A04 | 22047095 | G | A | synonymous_variant | LOW | c.363C>T|p.Ile121Ile |
S273 |
| 8 | BAA04g17980 | A04 | 22047448 | C | T | intron_variant | MODIFIER | c.146-53G>A| |
S159 |
| 9 | BAA04g17980 | A04 | 22047681 | C | T | missense_variant | MODERATE | c.40G>A|p.Glu14Lys |
S238 |
| 10 | BAA04g17980 | A04 | 22047795 | G | A | upstream_gene_variant | MODIFIER | c.-75C>T| |
S218 |
| 11 | BAA04g17980 | A04 | 22049076 | A | T | upstream_gene_variant | MODIFIER | c.-1356T>A| |
S94 |
| 12 | BAA04g17980 | A04 | 22049306 | G | A | upstream_gene_variant | MODIFIER | c.-1586C>T| |
S72 |
| 13 | BAA04g17980 | A04 | 22050084 | C | T | upstream_gene_variant | MODIFIER | c.-2364G>A| |
S183 S198 |
| 14 | BAA04g17980 | A04 | 22052018 | G | T | upstream_gene_variant | MODIFIER | c.-4298C>A| |
S114 |
| 15 | BAA04g17980 | A04 | 22052273 | G | A | upstream_gene_variant | MODIFIER | c.-4553C>T| |
S19 |
| 16 | BAA04g17980 | A04 | 22052378 | G | A | upstream_gene_variant | MODIFIER | c.-4658C>T| |
S34 |
| 17 | BAA04g17980 | A04 | 22052472 | C | T | upstream_gene_variant | MODIFIER | c.-4752G>A| |
S260 |