| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 39451 | BAA01g25260 | A01 | 13616641 | G | A | downstream_gene_variant | MODIFIER | c.*2346G>A| |
S274 |
| 39452 | BAA01g25260 | A01 | 13616777 | G | A | downstream_gene_variant | MODIFIER | c.*2482G>A| |
S105 S106 |
| 39453 | BAA01g25260 | A01 | 13616824 | G | A | downstream_gene_variant | MODIFIER | c.*2529G>A| |
S169 |
| 39454 | BAA01g25260 | A01 | 13617859 | G | A | downstream_gene_variant | MODIFIER | c.*3564G>A| |
S274 |
| 39455 | BAA01g25260 | A01 | 13619092 | C | T | downstream_gene_variant | MODIFIER | c.*4797C>T| |
S204 |
| 39456 | BAA01g25270 | A01 | 13620289 | G | A | downstream_gene_variant | MODIFIER | c.*686C>T| |
S109 |
| 39457 | BAA01g25270 | A01 | 13621526 | G | A | intron_variant | MODIFIER | c.2439+12C>T| |
S236 |
| 39458 | BAA01g25270 | A01 | 13621902 | C | T | missense_variant | MODERATE | c.2283G>A|p.Met761Ile |
S11 |
| 39459 | BAA01g25270 | A01 | 13622891 | C | T | intron_variant | MODIFIER | c.1808+17G>A| |
S249 |
| 39460 | BAA01g25270 | A01 | 13623105 | C | T | missense_variant | MODERATE | c.1715G>A|p.Arg572Lys |
S28 |
| 39461 | BAA01g25270 | A01 | 13623464 | G | A | intron_variant | MODIFIER | c.1662+77C>T| |
S23 |
| 39462 | BAA01g25270 | A01 | 13623767 | C | T | intron_variant | MODIFIER | c.1605-169G>A| |
S183 |
| 39463 | BAA01g25270 | A01 | 13624738 | C | T | missense_variant | MODERATE | c.1339G>A|p.Glu447Lys |
S249 |
| 39464 | BAA01g25270 | A01 | 13624833 | G | A | missense_variant | MODERATE | c.1244C>T|p.Ser415Phe |
S9 |
| 39465 | BAA01g25270 | A01 | 13625210 | G | A | synonymous_variant | LOW | c.1086C>T|p.Leu362Leu |
S236 |
| 39466 | BAA01g25280 | A01 | 13626090 | G | A | upstream_gene_variant | MODIFIER | c.-3739G>A| |
S59 |
| 39467 | BAA01g25270 | A01 | 13626684 | C | T | missense_variant | MODERATE | c.538G>A|p.Asp180Asn |
S67 |
| 39468 | BAA01g25280 | A01 | 13630024 | C | T | missense_variant | MODERATE | c.125C>T|p.Ala42Val |
S182 |
| 39469 | BAA01g25270 | A01 | 13632420 | C | T | upstream_gene_variant | MODIFIER | c.-4701G>A| |
S81 S85 |
| 39470 | BAA01g25270 | A01 | 13632581 | G | A | upstream_gene_variant | MODIFIER | c.-4862C>T| |
S189 S250 S41 |
| 39471 | BAA01g25280 | A01 | 13632623 | G | A | missense_variant | MODERATE | c.1156G>A|p.Ala386Thr |
S71 |
| 39472 | BAA01g25280 | A01 | 13632840 | G | A | intron_variant | MODIFIER | c.1324-42G>A| |
S275 |
| 39473 | BAA01g25280 | A01 | 13634055 | G | A | missense_variant | MODERATE | c.2081G>A|p.Arg694Lys |
S299 |
| 39474 | BAA01g25290 | A01 | 13634309 | C | T | upstream_gene_variant | MODIFIER | c.-4007C>T| |
S117 |
| 39475 | BAA01g25280 | A01 | 13634332 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2268-1G>A| |
S197 |