| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 145601 | BAA10g30120 | A10 | 22437837 | G | A | synonymous_variant | LOW | c.438C>T|p.Leu146Leu |
S178 |
| 145602 | BAA10g30120 | A10 | 22438187 | G | A | synonymous_variant | LOW | c.88C>T|p.Leu30Leu |
S81 |
| 145603 | BAA10g30120 | A10 | 22438265 | C | T | missense_variant | MODERATE | c.10G>A|p.Glu4Lys |
S56 |
| 145604 | BAA10g30120 | A10 | 22438947 | G | A | upstream_gene_variant | MODIFIER | c.-673C>T| |
S256 |
| 145605 | BAA10g30120 | A10 | 22439799 | G | A | upstream_gene_variant | MODIFIER | c.-1525C>T| |
S294 |
| 145606 | BAA10g30120 | A10 | 22441858 | C | T | upstream_gene_variant | MODIFIER | c.-3584G>A| |
S295 |
| 145607 | BAA10g30120 | A10 | 22442522 | G | A | upstream_gene_variant | MODIFIER | c.-4248C>T| |
S181 |
| 145608 | BAA10g30120 | A10 | 22442604 | G | A | upstream_gene_variant | MODIFIER | c.-4330C>T| |
S263 |
| 145609 | BAA10g30120 | A10 | 22442678 | C | T | upstream_gene_variant | MODIFIER | c.-4404G>A| |
S301 S304 |
| 145610 | BAA10g30120 | A10 | 22442782 | G | A | upstream_gene_variant | MODIFIER | c.-4508C>T| |
S264 |
| 145611 | BAA10g30130 | A10 | 22443901 | C | T | upstream_gene_variant | MODIFIER | c.-1451C>T| |
S297 |
| 145612 | BAA10g30130 | A10 | 22445203 | C | T | upstream_gene_variant | MODIFIER | c.-149C>T| |
S104 S52 |
| 145613 | BAA10g30130 | A10 | 22447524 | C | T | missense_variant | MODERATE | c.935C>T|p.Pro312Leu |
S148 S30 S31 |
| 145614 | BAA10g30130 | A10 | 22447883 | G | A | missense_variant | MODERATE | c.1294G>A|p.Gly432Ser |
S75 S81 |
| 145615 | BAA10g30150 | A10 | 22450226 | C | T | upstream_gene_variant | MODIFIER | c.-4768C>T| |
S167 |
| 145616 | BAA10g30150 | A10 | 22451135 | C | T | upstream_gene_variant | MODIFIER | c.-3859C>T| |
S308 |
| 145617 | BAA10g30140 | A10 | 22451938 | C | T | missense_variant | MODERATE | c.494G>A|p.Gly165Glu |
S269 |
| 145618 | BAA10g30140 | A10 | 22452413 | G | A | stop_gained | HIGH | c.115C>T|p.Gln39* |
S190 |
| 145619 | BAA10g30140 | A10 | 22452486 | G | A | synonymous_variant | LOW | c.42C>T|p.Val14Val |
S151 |
| 145620 | BAA10g30140 | A10 | 22453720 | G | A | upstream_gene_variant | MODIFIER | c.-1193C>T| |
S239 |
| 145621 | BAA10g30140 | A10 | 22454737 | G | A | upstream_gene_variant | MODIFIER | c.-2210C>T| |
S71 |
| 145622 | BAA10g30140 | A10 | 22454841 | C | T | upstream_gene_variant | MODIFIER | c.-2314G>A| |
S96 |
| 145623 | BAA10g30150 | A10 | 22455074 | G | A | stop_gained | HIGH | c.81G>A|p.Trp27* |
S263 |
| 145624 | BAA10g30150 | A10 | 22455322 | G | A | missense_variant | MODERATE | c.329G>A|p.Arg110Gln |
S209 |
| 145625 | BAA10g30140 | A10 | 22455396 | C | T | upstream_gene_variant | MODIFIER | c.-2869G>A| |
S67 |