| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 29751 | BAA01g20960 | A01 | 10321107 | G | A | missense_variant | MODERATE | c.701G>A|p.Ser234Asn |
S1 S90 |
| 29752 | BAA01g20970 | A01 | 10321707 | G | A | upstream_gene_variant | MODIFIER | c.-2225G>A| |
S173 |
| 29753 | BAA01g20970 | A01 | 10323166 | C | T | upstream_gene_variant | MODIFIER | c.-766C>T| |
S200 S247 |
| 29754 | BAA01g20970 | A01 | 10323335 | C | T | upstream_gene_variant | MODIFIER | c.-597C>T| |
S69 |
| 29755 | BAA01g20970 | A01 | 10324226 | G | A | missense_variant&splice_region_variant | MODERATE | c.197G>A|p.Ser66Asn |
S239 |
| 29756 | BAA01g20960 | A01 | 10325416 | C | T | downstream_gene_variant | MODIFIER | c.*2931C>T| |
S226 |
| 29757 | BAA01g20960 | A01 | 10326227 | G | A | downstream_gene_variant | MODIFIER | c.*3742G>A| |
S244 |
| 29758 | BAA01g20970 | A01 | 10326716 | C | T | synonymous_variant | LOW | c.1653C>T|p.Leu551Leu |
S277 |
| 29759 | BAA01g20980 | A01 | 10329065 | G | A | upstream_gene_variant | MODIFIER | c.-200C>T| |
S13 |
| 29760 | BAA01g20980 | A01 | 10329241 | C | T | upstream_gene_variant | MODIFIER | c.-376G>A| |
S50 |
| 29761 | BAA01g20980 | A01 | 10329347 | C | T | upstream_gene_variant | MODIFIER | c.-482G>A| |
S50 |
| 29762 | BAA01g20980 | A01 | 10329543 | G | C | upstream_gene_variant | MODIFIER | c.-678C>G| |
S192 |
| 29763 | BAA01g20980 | A01 | 10330145 | G | A | upstream_gene_variant | MODIFIER | c.-1280C>T| |
S45 |
| 29764 | BAA01g20980 | A01 | 10331095 | C | T | upstream_gene_variant | MODIFIER | c.-2230G>A| |
S35 |
| 29765 | BAA01g20980 | A01 | 10331124 | G | A | upstream_gene_variant | MODIFIER | c.-2259C>T| |
S84 S93 |
| 29766 | BAA01g20980 | A01 | 10331289 | G | A | upstream_gene_variant | MODIFIER | c.-2424C>T| |
S203 |
| 29767 | BAA01g20980 | A01 | 10331301 | G | A | upstream_gene_variant | MODIFIER | c.-2436C>T| |
S291 |
| 29768 | BAA01g20980 | A01 | 10331457 | C | T | upstream_gene_variant | MODIFIER | c.-2592G>A| |
S155 S211 |
| 29769 | BAA01g20990 | A01 | 10332215 | C | T | synonymous_variant | LOW | c.2946G>A|p.Thr982Thr |
S295 |
| 29770 | BAA01g20990 | A01 | 10332340 | C | T | missense_variant | MODERATE | c.2821G>A|p.Ala941Thr |
S10 |
| 29771 | BAA01g20990 | A01 | 10332411 | C | T | missense_variant | MODERATE | c.2750G>A|p.Arg917Lys |
S255 |
| 29772 | BAA01g20990 | A01 | 10333027 | C | T | missense_variant | MODERATE | c.2134G>A|p.Ala712Thr |
S65 |
| 29773 | BAA01g20980 | A01 | 10333302 | G | A | upstream_gene_variant | MODIFIER | c.-4437C>T| |
S169 |
| 29774 | BAA01g20980 | A01 | 10333326 | C | T | upstream_gene_variant | MODIFIER | c.-4461G>A| |
S261 |
| 29775 | BAA01g20990 | A01 | 10333388 | G | A | stop_gained | HIGH | c.1867C>T|p.Arg623* |
S308 |