| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 115201 | BAA10g09630 | A10 | 11561517 | C | T | upstream_gene_variant | MODIFIER | c.-687G>A| |
S104 S52 |
| 115202 | BAA10g09630 | A10 | 11563269 | G | A | upstream_gene_variant | MODIFIER | c.-2439C>T| |
S65 |
| 115203 | BAA10g09630 | A10 | 11563323 | G | A | upstream_gene_variant | MODIFIER | c.-2493C>T| |
S261 |
| 115204 | BAA10g09640 | A10 | 11563889 | G | A | missense_variant | MODERATE | c.34G>A|p.Glu12Lys |
S202 |
| 115205 | BAA10g09630 | A10 | 11565273 | G | A | upstream_gene_variant | MODIFIER | c.-4443C>T| |
S95 |
| 115206 | BAA10g09630 | A10 | 11565783 | C | T | upstream_gene_variant | MODIFIER | c.-4953G>A| |
S238 |
| 115207 | BAA10g09640 | A10 | 11569853 | G | A | downstream_gene_variant | MODIFIER | c.*1139G>A| |
S176 S184 |
| 115208 | BAA10g09640 | A10 | 11572485 | C | T | downstream_gene_variant | MODIFIER | c.*3771C>T| |
S281 |
| 115209 | BAA10g09640 | A10 | 11572966 | G | A | downstream_gene_variant | MODIFIER | c.*4252G>A| |
S13 |
| 115210 | BAA10g09650 | A10 | 11573330 | C | T | upstream_gene_variant | MODIFIER | c.-252G>A| |
S79 S91 |
| 115211 | BAA10g09650 | A10 | 11573361 | G | A | upstream_gene_variant | MODIFIER | c.-283C>T| |
S288 |
| 115212 | BAA10g09650 | A10 | 11574323 | G | A | upstream_gene_variant | MODIFIER | c.-1245C>T| |
S283 |
| 115213 | BAA10g09650 | A10 | 11574947 | G | A | upstream_gene_variant | MODIFIER | c.-1869C>T| |
S157 S166 S167 |
| 115214 | BAA10g09660 | A10 | 11578129 | C | T | downstream_gene_variant | MODIFIER | c.*3822G>A| |
S259 |
| 115215 | BAA10g09660 | A10 | 11579094 | G | A | downstream_gene_variant | MODIFIER | c.*2857C>T| |
S289 |
| 115216 | BAA10g09660 | A10 | 11580832 | C | T | downstream_gene_variant | MODIFIER | c.*1119G>A| |
S259 |
| 115217 | BAA10g09670 | A10 | 11582763 | C | T | upstream_gene_variant | MODIFIER | c.-4947C>T| |
S266 |
| 115218 | BAA10g09670 | A10 | 11582823 | G | A | upstream_gene_variant | MODIFIER | c.-4887G>A| |
S127 |
| 115219 | BAA10g09670 | A10 | 11583867 | C | T | upstream_gene_variant | MODIFIER | c.-3843C>T| |
S146 |
| 115220 | BAA10g09660 | A10 | 11584194 | C | T | missense_variant | MODERATE | c.226G>A|p.Ala76Thr |
S204 |
| 115221 | BAA10g09660 | A10 | 11585301 | G | A | upstream_gene_variant | MODIFIER | c.-600C>T| |
S13 S140 S279 S64 |
| 115222 | BAA10g09660 | A10 | 11586604 | C | T | upstream_gene_variant | MODIFIER | c.-1903G>A| |
S165 |
| 115223 | BAA10g09660 | A10 | 11587125 | G | A | upstream_gene_variant | MODIFIER | c.-2424C>T| |
S261 |
| 115224 | BAA10g09660 | A10 | 11587186 | G | A | upstream_gene_variant | MODIFIER | c.-2485C>T| |
S68 |
| 115225 | BAA10g09660 | A10 | 11589550 | C | T | upstream_gene_variant | MODIFIER | c.-4849G>A| |
S5 |