| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 27751 | BAA01g19650 | A01 | 9673597 | G | A | missense_variant&splice_region_variant | MODERATE | c.13G>A|p.Glu5Lys |
S165 |
| 27752 | BAA01g19650 | A01 | 9673786 | G | A | missense_variant | MODERATE | c.100G>A|p.Asp34Asn |
S162 |
| 27753 | BAA01g19650 | A01 | 9673864 | C | T | synonymous_variant | LOW | c.178C>T|p.Leu60Leu |
S55 |
| 27754 | BAA01g19640 | A01 | 9675897 | G | A | downstream_gene_variant | MODIFIER | c.*2618G>A| |
S287 |
| 27755 | BAA01g19650 | A01 | 9678488 | C | T | downstream_gene_variant | MODIFIER | c.*3316C>T| |
S155 |
| 27756 | BAA01g19660 | A01 | 9679781 | G | A | upstream_gene_variant | MODIFIER | c.-4287G>A| |
S163 |
| 27757 | BAA01g19660 | A01 | 9682243 | G | A | upstream_gene_variant | MODIFIER | c.-1825G>A| |
S183 |
| 27758 | BAA01g19660 | A01 | 9684292 | G | A | synonymous_variant | LOW | c.225G>A|p.Gln75Gln |
S236 |
| 27759 | BAA01g19660 | A01 | 9684440 | C | T | missense_variant | MODERATE | c.373C>T|p.His125Tyr |
S167 |
| 27760 | BAA01g19660 | A01 | 9684493 | C | T | synonymous_variant | LOW | c.426C>T|p.Asp142Asp |
S100 |
| 27761 | BAA01g19660 | A01 | 9684524 | G | A | missense_variant | MODERATE | c.457G>A|p.Val153Ile |
S139 |
| 27762 | BAA01g19660 | A01 | 9684526 | C | T | synonymous_variant | LOW | c.459C>T|p.Val153Val |
S78 |
| 27763 | BAA01g19660 | A01 | 9684660 | C | T | missense_variant | MODERATE | c.593C>T|p.Pro198Leu |
S134 |
| 27764 | BAA01g19660 | A01 | 9685427 | G | A | downstream_gene_variant | MODIFIER | c.*28G>A| |
S296 |
| 27765 | BAA01g19670 | A01 | 9686268 | C | T | missense_variant | MODERATE | c.628G>A|p.Ala210Thr |
S8 |
| 27766 | BAA01g19670 | A01 | 9686309 | G | A | missense_variant | MODERATE | c.587C>T|p.Ala196Val |
S32 |
| 27767 | BAA01g19670 | A01 | 9686547 | G | A | missense_variant | MODERATE | c.349C>T|p.Leu117Phe |
S249 |
| 27768 | BAA01g19660 | A01 | 9686844 | G | A | downstream_gene_variant | MODIFIER | c.*1445G>A| |
S60 |
| 27769 | BAA01g19660 | A01 | 9687038 | G | A | downstream_gene_variant | MODIFIER | c.*1639G>A| |
S168 |
| 27770 | BAA01g19660 | A01 | 9687071 | G | A | downstream_gene_variant | MODIFIER | c.*1672G>A| |
S6 |
| 27771 | BAA01g19670 | A01 | 9687220 | C | T | missense_variant | MODERATE | c.56G>A|p.Gly19Asp |
S166 |
| 27772 | BAA01g19670 | A01 | 9687482 | C | T | upstream_gene_variant | MODIFIER | c.-207G>A| |
S104 S52 |
| 27773 | BAA01g19670 | A01 | 9688534 | C | T | upstream_gene_variant | MODIFIER | c.-1259G>A| |
S134 |
| 27774 | BAA01g19670 | A01 | 9689297 | G | A | upstream_gene_variant | MODIFIER | c.-2022C>T| |
S278 |
| 27775 | BAA01g19670 | A01 | 9690105 | C | T | upstream_gene_variant | MODIFIER | c.-2830G>A| |
S210 S225 |