| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 193551 | BAA02g27430 | A02 | 15438681 | C | T | downstream_gene_variant | MODIFIER | c.*3472G>A| |
S284 |
| 193552 | BAA02g27430 | A02 | 15439976 | G | A | downstream_gene_variant | MODIFIER | c.*2177C>T| |
S134 |
| 193553 | BAA02g27430 | A02 | 15441480 | C | T | downstream_gene_variant | MODIFIER | c.*673G>A| |
S265 S39 |
| 193554 | BAA02g27430 | A02 | 15441665 | C | T | downstream_gene_variant | MODIFIER | c.*488G>A| |
S271 |
| 193555 | BAA02g27430 | A02 | 15442005 | G | A | downstream_gene_variant | MODIFIER | c.*148C>T| |
S232 |
| 193556 | BAA02g27430 | A02 | 15442202 | G | A | missense_variant | MODERATE | c.1001C>T|p.Pro334Leu |
S229 |
| 193557 | BAA02g27430 | A02 | 15442702 | C | T | synonymous_variant | LOW | c.501G>A|p.Lys167Lys |
S40 S49 |
| 193558 | BAA02g27430 | A02 | 15443255 | G | A | intron_variant | MODIFIER | c.191-119C>T| |
S168 |
| 193559 | BAA02g27430 | A02 | 15446490 | C | T | upstream_gene_variant | MODIFIER | c.-2525G>A| |
S46 |
| 193560 | BAA02g27430 | A02 | 15446993 | G | A | upstream_gene_variant | MODIFIER | c.-3028C>T| |
S28 |
| 193561 | BAA02g27430 | A02 | 15448047 | C | T | upstream_gene_variant | MODIFIER | c.-4082G>A| |
S131 |
| 193562 | BAA02g27460 | A02 | 15449799 | G | A | upstream_gene_variant | MODIFIER | c.-2814G>A| |
S61 |
| 193563 | BAA02g27450 | A02 | 15450711 | C | T | synonymous_variant | LOW | c.1680G>A|p.Gln560Gln |
S46 |
| 193564 | BAA02g27450 | A02 | 15450829 | G | A | missense_variant | MODERATE | c.1562C>T|p.Pro521Leu |
S143 |
| 193565 | BAA02g27450 | A02 | 15451310 | G | A | missense_variant | MODERATE | c.1081C>T|p.Leu361Phe |
S241 |
| 193566 | BAA02g27450 | A02 | 15451328 | C | T | missense_variant | MODERATE | c.1063G>A|p.Gly355Ser |
S77 S82 |
| 193567 | BAA02g27450 | A02 | 15451565 | C | T | missense_variant | MODERATE | c.826G>A|p.Val276Ile |
S179 |
| 193568 | BAA02g27450 | A02 | 15451605 | G | A | synonymous_variant | LOW | c.786C>T|p.Phe262Phe |
S50 |
| 193569 | BAA02g27450 | A02 | 15451675 | C | T | missense_variant | MODERATE | c.716G>A|p.Arg239Lys |
S167 |
| 193570 | BAA02g27460 | A02 | 15451832 | C | T | upstream_gene_variant | MODIFIER | c.-781C>T| |
S221 |
| 193571 | BAA02g27450 | A02 | 15452317 | G | A | missense_variant | MODERATE | c.239C>T|p.Ala80Val |
S223 |
| 193572 | BAA02g27450 | A02 | 15452454 | G | A | synonymous_variant | LOW | c.102C>T|p.Phe34Phe |
S184 |
| 193573 | BAA02g27450 | A02 | 15453549 | G | A | upstream_gene_variant | MODIFIER | c.-994C>T| |
S19 |
| 193574 | BAA02g27450 | A02 | 15453580 | G | A | upstream_gene_variant | MODIFIER | c.-1025C>T| |
S197 |
| 193575 | BAA02g27450 | A02 | 15454442 | G | A | upstream_gene_variant | MODIFIER | c.-1887C>T| |
S67 |