| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 52251 | BAA01g28800 | A01 | 18098431 | G | A | upstream_gene_variant | MODIFIER | c.-1363C>T| |
S287 |
| 52252 | BAA01g28800 | A01 | 18098484 | C | T | upstream_gene_variant | MODIFIER | c.-1416G>A| |
S206 |
| 52253 | BAA01g28800 | A01 | 18099266 | C | T | upstream_gene_variant | MODIFIER | c.-2198G>A| |
S255 |
| 52254 | BAA01g28800 | A01 | 18101060 | G | A | upstream_gene_variant | MODIFIER | c.-3992C>T| |
S155 |
| 52255 | BAA01g28800 | A01 | 18101237 | C | T | upstream_gene_variant | MODIFIER | c.-4169G>A| |
S142 |
| 52256 | BAA01g28800 | A01 | 18101341 | G | T | upstream_gene_variant | MODIFIER | c.-4273C>A| |
S210 |
| 52257 | BAA01g28810 | A01 | 18102600 | G | A | downstream_gene_variant | MODIFIER | c.*2278C>T| |
S178 |
| 52258 | BAA01g28810 | A01 | 18102965 | G | A | downstream_gene_variant | MODIFIER | c.*1913C>T| |
S262 |
| 52259 | BAA01g28810 | A01 | 18103271 | G | A | downstream_gene_variant | MODIFIER | c.*1607C>T| |
S149 |
| 52260 | BAA01g28820 | A01 | 18104302 | C | T | upstream_gene_variant | MODIFIER | c.-4781C>T| |
S200 |
| 52261 | BAA01g28810 | A01 | 18105618 | C | T | missense_variant | MODERATE | c.439G>A|p.Ala147Thr |
S206 S26 |
| 52262 | BAA01g28810 | A01 | 18105757 | G | A | synonymous_variant | LOW | c.300C>T|p.Phe100Phe |
S55 |
| 52263 | BAA01g28810 | A01 | 18106517 | C | T | upstream_gene_variant | MODIFIER | c.-368G>A| |
S203 |
| 52264 | BAA01g28810 | A01 | 18107145 | G | A | upstream_gene_variant | MODIFIER | c.-996C>T| |
S109 |
| 52265 | BAA01g28810 | A01 | 18108203 | C | T | upstream_gene_variant | MODIFIER | c.-2054G>A| |
S82 S92 |
| 52266 | BAA01g28810 | A01 | 18108359 | C | T | upstream_gene_variant | MODIFIER | c.-2210G>A| |
S130 |
| 52267 | BAA01g28820 | A01 | 18110641 | C | T | missense_variant | MODERATE | c.662C>T|p.Ser221Phe |
S204 |
| 52268 | BAA01g28820 | A01 | 18110722 | C | T | missense_variant | MODERATE | c.743C>T|p.Thr248Met |
S167 |
| 52269 | BAA01g28820 | A01 | 18112998 | G | A | intron_variant | MODIFIER | c.970+810G>A| |
S207 |
| 52270 | BAA01g28820 | A01 | 18113318 | G | A | intron_variant | MODIFIER | c.970+1130G>A| |
S124 |
| 52271 | BAA01g28820 | A01 | 18113770 | G | A | intron_variant | MODIFIER | c.970+1582G>A| |
S9 |
| 52272 | BAA01g28820 | A01 | 18115539 | C | T | intron_variant | MODIFIER | c.970+3351C>T| |
S205 |
| 52273 | BAA01g28820 | A01 | 18115970 | G | A | intron_variant | MODIFIER | c.970+3782G>A| |
S308 |
| 52274 | BAA01g28820 | A01 | 18117119 | G | A | intron_variant | MODIFIER | c.970+4931G>A| |
S12 |
| 52275 | BAA01g28820 | A01 | 18117461 | A | C | intron_variant | MODIFIER | c.971-4769A>C| |
S58 |