| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 134551 | BAA10g20720 | A10 | 18512005 | A | T | synonymous_variant | LOW | c.1095A>T|p.Gly365Gly |
S1 S90 |
| 134552 | BAA10g20730 | A10 | 18512900 | G | A | upstream_gene_variant | MODIFIER | c.-324G>A| |
S255 |
| 134553 | BAA10g20720 | A10 | 18513916 | C | T | downstream_gene_variant | MODIFIER | c.*1653C>T| |
S61 |
| 134554 | BAA10g20730 | A10 | 18514188 | G | A | stop_gained | HIGH | c.504G>A|p.Trp168* |
S207 |
| 134555 | BAA10g20730 | A10 | 18514452 | C | T | synonymous_variant | LOW | c.666C>T|p.Cys222Cys |
S268 |
| 134556 | BAA10g20730 | A10 | 18514611 | G | A | synonymous_variant | LOW | c.825G>A|p.Arg275Arg |
S158 |
| 134557 | BAA10g20750 | A10 | 18517336 | C | T | missense_variant | MODERATE | c.1792G>A|p.Asp598Asn |
S2 |
| 134558 | BAA10g20750 | A10 | 18517862 | G | A | missense_variant | MODERATE | c.1429C>T|p.Pro477Ser |
S165 |
| 134559 | BAA10g20740 | A10 | 18518800 | C | T | upstream_gene_variant | MODIFIER | c.-1887G>A| |
S68 |
| 134560 | BAA10g20750 | A10 | 18519382 | C | T | synonymous_variant | LOW | c.471G>A|p.Leu157Leu |
S45 |
| 134561 | BAA10g20750 | A10 | 18519706 | G | A | synonymous_variant | LOW | c.147C>T|p.Arg49Arg |
S216 |
| 134562 | BAA10g20740 | A10 | 18519855 | G | A | upstream_gene_variant | MODIFIER | c.-2942C>T| |
S295 |
| 134563 | BAA10g20740 | A10 | 18520739 | G | A | upstream_gene_variant | MODIFIER | c.-3826C>T| |
S293 |
| 134564 | BAA10g20750 | A10 | 18522122 | G | A | upstream_gene_variant | MODIFIER | c.-2270C>T| |
S167 |
| 134565 | BAA10g20750 | A10 | 18523536 | G | A | upstream_gene_variant | MODIFIER | c.-3684C>T| |
S278 |
| 134566 | BAA10g20750 | A10 | 18524767 | T | C | upstream_gene_variant | MODIFIER | c.-4915A>G| |
S19 |
| 134567 | BAA10g20760 | A10 | 18525691 | G | A | upstream_gene_variant | MODIFIER | c.-2638C>T| |
S264 |
| 134568 | BAA10g20760 | A10 | 18525851 | C | A | upstream_gene_variant | MODIFIER | c.-2798G>T| |
S305 |
| 134569 | BAA10g20770 | A10 | 18526165 | C | T | missense_variant | MODERATE | c.7C>T|p.Pro3Ser |
S201 |
| 134570 | BAA10g20770 | A10 | 18526585 | C | T | synonymous_variant | LOW | c.213C>T|p.Asn71Asn |
S54 |
| 134571 | BAA10g20770 | A10 | 18526908 | C | T | synonymous_variant | LOW | c.448C>T|p.Leu150Leu |
S169 |
| 134572 | BAA10g20770 | A10 | 18526935 | G | A | missense_variant | MODERATE | c.475G>A|p.Asp159Asn |
S286 |
| 134573 | BAA10g20760 | A10 | 18527077 | G | A | upstream_gene_variant | MODIFIER | c.-4024C>T| |
S35 |
| 134574 | BAA10g20770 | A10 | 18527106 | G | A | synonymous_variant | LOW | c.522G>A|p.Gln174Gln |
S74 |
| 134575 | BAA10g20760 | A10 | 18527483 | G | A | upstream_gene_variant | MODIFIER | c.-4430C>T| |
S192 |