| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 133551 | BAA10g19990 | A10 | 18160138 | G | A | upstream_gene_variant | MODIFIER | c.-3425G>A| |
S1 S90 |
| 133552 | BAA10g19990 | A10 | 18160756 | C | T | upstream_gene_variant | MODIFIER | c.-2807C>T| |
S199 |
| 133553 | BAA10g19990 | A10 | 18160757 | G | A | upstream_gene_variant | MODIFIER | c.-2806G>A| |
S63 |
| 133554 | BAA10g19990 | A10 | 18161511 | G | A | upstream_gene_variant | MODIFIER | c.-2052G>A| |
S283 |
| 133555 | BAA10g19990 | A10 | 18161960 | C | T | upstream_gene_variant | MODIFIER | c.-1603C>T| |
S286 |
| 133556 | BAA10g19990 | A10 | 18163214 | G | A | upstream_gene_variant | MODIFIER | c.-349G>A| |
S131 |
| 133557 | BAA10g19990 | A10 | 18163702 | G | A | missense_variant | MODERATE | c.140G>A|p.Cys47Tyr |
S231 |
| 133558 | BAA10g19990 | A10 | 18163759 | C | T | missense_variant | MODERATE | c.197C>T|p.Ala66Val |
S152 |
| 133559 | BAA10g19990 | A10 | 18163919 | C | T | synonymous_variant | LOW | c.357C>T|p.Gly119Gly |
S210 S225 |
| 133560 | BAA10g19990 | A10 | 18163944 | G | A | missense_variant | MODERATE | c.382G>A|p.Gly128Ser |
S66 |
| 133561 | BAA10g20000 | A10 | 18164650 | C | T | upstream_gene_variant | MODIFIER | c.-3894C>T| |
S199 |
| 133562 | BAA10g20000 | A10 | 18165324 | C | T | upstream_gene_variant | MODIFIER | c.-3220C>T| |
S305 |
| 133563 | BAA10g20000 | A10 | 18165386 | C | T | upstream_gene_variant | MODIFIER | c.-3158C>T| |
S99 |
| 133564 | BAA10g20000 | A10 | 18165670 | G | A | upstream_gene_variant | MODIFIER | c.-2874G>A| |
S239 |
| 133565 | BAA10g20000 | A10 | 18166436 | G | A | upstream_gene_variant | MODIFIER | c.-2108G>A| |
S284 |
| 133566 | BAA10g20000 | A10 | 18166717 | C | T | upstream_gene_variant | MODIFIER | c.-1827C>T| |
S99 |
| 133567 | BAA10g20000 | A10 | 18167636 | A | G | upstream_gene_variant | MODIFIER | c.-908A>G| |
S147 S151 S199 S229 |
| 133568 | BAA10g20000 | A10 | 18168993 | G | A | missense_variant | MODERATE | c.152G>A|p.Ser51Asn |
S67 |
| 133569 | BAA10g20000 | A10 | 18170341 | G | A | missense_variant | MODERATE | c.919G>A|p.Gly307Arg |
S223 |
| 133570 | BAA10g20000 | A10 | 18171305 | C | T | stop_gained | HIGH | c.1705C>T|p.Gln569* |
S204 |
| 133571 | BAA10g20000 | A10 | 18171737 | C | T | synonymous_variant | LOW | c.2137C>T|p.Leu713Leu |
S44 |
| 133572 | BAA10g20000 | A10 | 18173465 | C | T | downstream_gene_variant | MODIFIER | c.*111C>T| |
S268 |
| 133573 | BAA10g20000 | A10 | 18173498 | C | T | downstream_gene_variant | MODIFIER | c.*144C>T| |
S87 |
| 133574 | BAA10g20000 | A10 | 18174069 | G | A | downstream_gene_variant | MODIFIER | c.*715G>A| |
S291 |
| 133575 | BAA10g20010 | A10 | 18174118 | G | A | synonymous_variant | LOW | c.489C>T|p.Arg163Arg |
S166 |