| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 81351 | BAA01g43030 | A01 | 28481020 | G | A | missense_variant | MODERATE | c.187G>A|p.Glu63Lys |
S149 |
| 81352 | BAA01g43030 | A01 | 28481647 | G | A | missense_variant | MODERATE | c.658G>A|p.Asp220Asn |
S95 |
| 81353 | BAA01g43040 | A01 | 28482674 | A | C | missense_variant | MODERATE | c.241A>C|p.Met81Leu |
S110 S138 S242 S274 |
| 81354 | BAA01g43020 | A01 | 28482985 | G | A | upstream_gene_variant | MODIFIER | c.-2595C>T| |
S246 S34 |
| 81355 | BAA01g43020 | A01 | 28483065 | G | A | upstream_gene_variant | MODIFIER | c.-2675C>T| |
S243 S299 |
| 81356 | BAA01g43040 | A01 | 28483718 | C | T | missense_variant | MODERATE | c.389C>T|p.Thr130Ile |
S177 |
| 81357 | BAA01g43040 | A01 | 28484333 | C | T | missense_variant | MODERATE | c.833C>T|p.Ala278Val |
S290 |
| 81358 | BAA01g43040 | A01 | 28484368 | G | A | missense_variant | MODERATE | c.868G>A|p.Gly290Ser |
S34 |
| 81359 | BAA01g43020 | A01 | 28485269 | C | T | upstream_gene_variant | MODIFIER | c.-4879G>A| |
S46 |
| 81360 | BAA01g43050 | A01 | 28485601 | C | T | upstream_gene_variant | MODIFIER | c.-82C>T| |
S44 |
| 81361 | BAA01g43050 | A01 | 28485963 | C | T | missense_variant | MODERATE | c.197C>T|p.Thr66Ile |
S47 |
| 81362 | BAA01g43050 | A01 | 28486778 | C | T | synonymous_variant | LOW | c.534C>T|p.Asp178Asp |
S170 |
| 81363 | BAA01g43050 | A01 | 28487360 | G | A | missense_variant | MODERATE | c.772G>A|p.Asp258Asn |
S287 |
| 81364 | BAA01g43050 | A01 | 28487754 | C | T | missense_variant | MODERATE | c.1166C>T|p.Ser389Phe |
S53 S75 S81 |
| 81365 | BAA01g43070 | A01 | 28488500 | G | A | upstream_gene_variant | MODIFIER | c.-2434G>A| |
S1 |
| 81366 | BAA01g43050 | A01 | 28489635 | C | T | missense_variant | MODERATE | c.2348C>T|p.Ser783Phe |
S286 |
| 81367 | BAA01g43070 | A01 | 28492772 | C | T | synonymous_variant | LOW | c.1146C>T|p.Asn382Asn |
S17 |
| 81368 | BAA01g43070 | A01 | 28492816 | C | T | missense_variant | MODERATE | c.1190C>T|p.Ala397Val |
S261 |
| 81369 | BAA01g43070 | A01 | 28492874 | G | A | synonymous_variant | LOW | c.1248G>A|p.Arg416Arg |
S144 |
| 81370 | BAA01g43070 | A01 | 28493462 | G | A | synonymous_variant | LOW | c.1623G>A|p.Ala541Ala |
S302 S8 |
| 81371 | BAA01g43060 | A01 | 28494367 | G | A | upstream_gene_variant | MODIFIER | c.-3784C>T| |
S244 |
| 81372 | BAA01g43070 | A01 | 28495921 | G | A | missense_variant | MODERATE | c.3103G>A|p.Val1035Ile |
S225 S73 |
| 81373 | BAA01g43080 | A01 | 28496616 | G | A | upstream_gene_variant | MODIFIER | c.-4621G>A| |
S197 |
| 81374 | BAA01g43080 | A01 | 28496673 | C | T | upstream_gene_variant | MODIFIER | c.-4564C>T| |
S249 |
| 81375 | BAA01g43080 | A01 | 28497004 | C | T | upstream_gene_variant | MODIFIER | c.-4233C>T| |
S153 S213 |