| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 114251 | BAA10g09230 | A10 | 11248497 | C | T | upstream_gene_variant | MODIFIER | c.-4919C>T| |
S165 S44 |
| 114252 | BAA10g09230 | A10 | 11248643 | G | A | upstream_gene_variant | MODIFIER | c.-4773G>A| |
S112 |
| 114253 | BAA10g09230 | A10 | 11249450 | C | T | upstream_gene_variant | MODIFIER | c.-3966C>T| |
S5 |
| 114254 | BAA10g09230 | A10 | 11249857 | C | T | upstream_gene_variant | MODIFIER | c.-3559C>T| |
S113 |
| 114255 | BAA10g09230 | A10 | 11250722 | G | A | upstream_gene_variant | MODIFIER | c.-2694G>A| |
S295 |
| 114256 | BAA10g09230 | A10 | 11251137 | C | T | upstream_gene_variant | MODIFIER | c.-2279C>T| |
S281 |
| 114257 | BAA10g09230 | A10 | 11251478 | C | T | upstream_gene_variant | MODIFIER | c.-1938C>T| |
S249 |
| 114258 | BAA10g09220 | A10 | 11251730 | C | T | missense_variant | MODERATE | c.406G>A|p.Asp136Asn |
S20 |
| 114259 | BAA10g09220 | A10 | 11251733 | C | T | missense_variant | MODERATE | c.403G>A|p.Val135Met |
S259 |
| 114260 | BAA10g09220 | A10 | 11251766 | C | T | missense_variant | MODERATE | c.370G>A|p.Glu124Lys |
S70 |
| 114261 | BAA10g09230 | A10 | 11251949 | C | T | upstream_gene_variant | MODIFIER | c.-1467C>T| |
S274 S303 |
| 114262 | BAA10g09220 | A10 | 11252096 | C | T | missense_variant&splice_region_variant | MODERATE | c.223G>A|p.Val75Ile |
S10 |
| 114263 | BAA10g09220 | A10 | 11252881 | G | A | upstream_gene_variant | MODIFIER | c.-345C>T| |
S13 |
| 114264 | BAA10g09220 | A10 | 11253206 | G | A | upstream_gene_variant | MODIFIER | c.-670C>T| |
S192 |
| 114265 | BAA10g09220 | A10 | 11253213 | G | A | upstream_gene_variant | MODIFIER | c.-677C>T| |
S150 |
| 114266 | BAA10g09230 | A10 | 11253486 | C | T | missense_variant | MODERATE | c.71C>T|p.Ser24Phe |
S123 |
| 114267 | BAA10g09230 | A10 | 11253686 | C | T | splice_region_variant&intron_variant | LOW | c.181+8C>T| |
S6 |
| 114268 | BAA10g09220 | A10 | 11253695 | C | T | upstream_gene_variant | MODIFIER | c.-1159G>A| |
S246 |
| 114269 | BAA10g09230 | A10 | 11254064 | G | A | missense_variant | MODERATE | c.395G>A|p.Cys132Tyr |
S226 |
| 114270 | BAA10g09220 | A10 | 11254192 | C | T | upstream_gene_variant | MODIFIER | c.-1656G>A| |
S235 |
| 114271 | BAA10g09220 | A10 | 11255681 | C | T | upstream_gene_variant | MODIFIER | c.-3145G>A| |
S191 |
| 114272 | BAA10g09240 | A10 | 11257727 | C | T | upstream_gene_variant | MODIFIER | c.-731G>A| |
S197 |
| 114273 | BAA10g09240 | A10 | 11257938 | C | T | upstream_gene_variant | MODIFIER | c.-942G>A| |
S238 |
| 114274 | BAA10g09240 | A10 | 11258547 | C | T | upstream_gene_variant | MODIFIER | c.-1551G>A| |
S166 |
| 114275 | BAA10g09240 | A10 | 11258597 | G | A | upstream_gene_variant | MODIFIER | c.-1601C>T| |
S151 S263 |