| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 48301 | BAA01g27770 | A01 | 16769702 | C | T | upstream_gene_variant | MODIFIER | c.-274C>T| |
S286 |
| 48302 | BAA01g27770 | A01 | 16770208 | G | A | missense_variant | MODERATE | c.145G>A|p.Val49Met |
S138 |
| 48303 | BAA01g27770 | A01 | 16770276 | C | T | synonymous_variant | LOW | c.213C>T|p.Cys71Cys |
S46 |
| 48304 | BAA01g27770 | A01 | 16770370 | C | T | missense_variant | MODERATE | c.307C>T|p.Leu103Phe |
S282 |
| 48305 | BAA01g27770 | A01 | 16770426 | C | T | synonymous_variant | LOW | c.363C>T|p.Tyr121Tyr |
S282 |
| 48306 | BAA01g27770 | A01 | 16770777 | A | T | missense_variant | MODERATE | c.714A>T|p.Glu238Asp |
S159 S243 |
| 48307 | BAA01g27770 | A01 | 16771132 | G | A | missense_variant | MODERATE | c.910G>A|p.Val304Ile |
S32 |
| 48308 | BAA01g27770 | A01 | 16771638 | C | T | missense_variant | MODERATE | c.1352C>T|p.Thr451Ile |
S242 |
| 48309 | BAA01g27770 | A01 | 16771879 | C | T | missense_variant | MODERATE | c.1478C>T|p.Ser493Phe |
S303 |
| 48310 | BAA01g27770 | A01 | 16771889 | C | T | synonymous_variant | LOW | c.1488C>T|p.His496His |
S69 |
| 48311 | BAA01g27770 | A01 | 16771948 | A | G | missense_variant | MODERATE | c.1547A>G|p.Asn516Ser |
S257 |
| 48312 | BAA01g27770 | A01 | 16772240 | C | T | missense_variant | MODERATE | c.1724C>T|p.Ser575Phe |
S48 |
| 48313 | BAA01g27770 | A01 | 16772293 | C | T | missense_variant | MODERATE | c.1777C>T|p.His593Tyr |
S10 |
| 48314 | BAA01g27770 | A01 | 16773484 | G | A | missense_variant | MODERATE | c.2515G>A|p.Ala839Thr |
S86 |
| 48315 | BAA01g27770 | A01 | 16773666 | C | T | synonymous_variant | LOW | c.2697C>T|p.His899His |
S294 |
| 48316 | BAA01g27780 | A01 | 16774133 | G | A | downstream_gene_variant | MODIFIER | c.*2027C>T| |
S25 |
| 48317 | BAA01g27780 | A01 | 16774442 | C | T | downstream_gene_variant | MODIFIER | c.*1718G>A| |
S158 |
| 48318 | BAA01g27770 | A01 | 16774585 | C | T | synonymous_variant | LOW | c.3024C>T|p.Phe1008Phe |
S119 |
| 48319 | BAA01g27770 | A01 | 16774781 | G | A | missense_variant | MODERATE | c.3220G>A|p.Ala1074Thr |
S202 |
| 48320 | BAA01g27770 | A01 | 16775060 | C | T | downstream_gene_variant | MODIFIER | c.*274C>T| |
S179 |
| 48321 | BAA01g27770 | A01 | 16775475 | C | T | downstream_gene_variant | MODIFIER | c.*689C>T| |
S234 |
| 48322 | BAA01g27770 | A01 | 16775607 | G | A | downstream_gene_variant | MODIFIER | c.*821G>A| |
S163 |
| 48323 | BAA01g27770 | A01 | 16777076 | G | A | downstream_gene_variant | MODIFIER | c.*2290G>A| |
S61 |
| 48324 | BAA01g27770 | A01 | 16777491 | C | T | downstream_gene_variant | MODIFIER | c.*2705C>T| |
S168 |
| 48325 | BAA01g27770 | A01 | 16777503 | G | A | downstream_gene_variant | MODIFIER | c.*2717G>A| |
S23 |