| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 72251 | BAA01g37750 | A01 | 25260179 | C | T | upstream_gene_variant | MODIFIER | c.-4424G>A| |
S249 |
| 72252 | BAA01g37760 | A01 | 25261821 | C | T | upstream_gene_variant | MODIFIER | c.-3511G>A| |
S200 |
| 72253 | BAA01g37760 | A01 | 25261822 | C | T | upstream_gene_variant | MODIFIER | c.-3512G>A| |
S75 S81 |
| 72254 | BAA01g37760 | A01 | 25261923 | G | A | upstream_gene_variant | MODIFIER | c.-3613C>T| |
S152 |
| 72255 | BAA01g37760 | A01 | 25262010 | C | T | upstream_gene_variant | MODIFIER | c.-3700G>A| |
S133 |
| 72256 | BAA01g37760 | A01 | 25262534 | G | A | upstream_gene_variant | MODIFIER | c.-4224C>T| |
S236 |
| 72257 | BAA01g37770 | A01 | 25263068 | G | A | missense_variant | MODERATE | c.707C>T|p.Ser236Phe |
S190 |
| 72258 | BAA01g37770 | A01 | 25264097 | G | A | upstream_gene_variant | MODIFIER | c.-323C>T| |
S284 |
| 72259 | BAA01g37770 | A01 | 25264433 | C | T | upstream_gene_variant | MODIFIER | c.-659G>A| |
S64 |
| 72260 | BAA01g37770 | A01 | 25264842 | C | T | upstream_gene_variant | MODIFIER | c.-1068G>A| |
S205 |
| 72261 | BAA01g37770 | A01 | 25265059 | C | T | upstream_gene_variant | MODIFIER | c.-1285G>A| |
S12 |
| 72262 | BAA01g37780 | A01 | 25265249 | C | T | missense_variant | MODERATE | c.67G>A|p.Val23Met |
S130 |
| 72263 | BAA01g37770 | A01 | 25267593 | C | T | upstream_gene_variant | MODIFIER | c.-3819G>A| |
S269 |
| 72264 | BAA01g37770 | A01 | 25267637 | C | T | upstream_gene_variant | MODIFIER | c.-3863G>A| |
S162 |
| 72265 | BAA01g37770 | A01 | 25267704 | C | T | upstream_gene_variant | MODIFIER | c.-3930G>A| |
S134 |
| 72266 | BAA01g37800 | A01 | 25271697 | C | T | upstream_gene_variant | MODIFIER | c.-1054G>A| |
S264 |
| 72267 | BAA01g37810 | A01 | 25271751 | C | G | missense_variant | MODERATE | c.541G>C|p.Gly181Arg |
S306 S308 |
| 72268 | BAA01g37810 | A01 | 25272322 | C | T | missense_variant&splice_region_variant | MODERATE | c.275G>A|p.Gly92Glu |
S79 |
| 72269 | BAA01g37810 | A01 | 25272609 | G | A | missense_variant | MODERATE | c.131C>T|p.Pro44Leu |
S283 |
| 72270 | BAA01g37800 | A01 | 25272662 | C | T | upstream_gene_variant | MODIFIER | c.-2019G>A| |
S208 |
| 72271 | BAA01g37800 | A01 | 25273484 | C | T | upstream_gene_variant | MODIFIER | c.-2841G>A| |
S127 |
| 72272 | BAA01g37810 | A01 | 25276112 | G | A | upstream_gene_variant | MODIFIER | c.-3291C>T| |
S169 |
| 72273 | BAA01g37810 | A01 | 25276716 | G | A | upstream_gene_variant | MODIFIER | c.-3895C>T| |
S271 |
| 72274 | BAA01g37810 | A01 | 25277408 | G | A | upstream_gene_variant | MODIFIER | c.-4587C>T| |
S80 S84 S86 S90 S93 |
| 72275 | BAA01g37830 | A01 | 25278655 | C | T | missense_variant | MODERATE | c.239G>A|p.Gly80Asp |
S179 |