| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 15451 | BAA01g11850 | A01 | 5541346 | G | A | intron_variant | MODIFIER | c.1325-69G>A| |
S161 |
| 15452 | BAA01g11850 | A01 | 5541634 | C | T | intron_variant | MODIFIER | c.1414-62C>T| |
S130 |
| 15453 | BAA01g11850 | A01 | 5542197 | C | T | synonymous_variant | LOW | c.1809C>T|p.Thr603Thr |
S155 |
| 15454 | BAA01g11860 | A01 | 5542524 | C | T | downstream_gene_variant | MODIFIER | c.*4437G>A| |
S233 |
| 15455 | BAA01g11850 | A01 | 5542741 | G | A | missense_variant | MODERATE | c.1969G>A|p.Asp657Asn |
S79 S91 |
| 15456 | BAA01g11850 | A01 | 5542916 | C | T | missense_variant | MODERATE | c.2144C>T|p.Ser715Phe |
S143 |
| 15457 | BAA01g11850 | A01 | 5543020 | G | A | missense_variant | MODERATE | c.2248G>A|p.Ala750Thr |
S232 |
| 15458 | BAA01g11850 | A01 | 5543057 | G | A | missense_variant | MODERATE | c.2285G>A|p.Gly762Asp |
S10 |
| 15459 | BAA01g11850 | A01 | 5544086 | G | A | synonymous_variant | LOW | c.2628G>A|p.Arg876Arg |
S157 S163 |
| 15460 | BAA01g11850 | A01 | 5544122 | G | A | synonymous_variant | LOW | c.2664G>A|p.Gln888Gln |
S165 |
| 15461 | BAA01g11860 | A01 | 5544473 | G | A | downstream_gene_variant | MODIFIER | c.*2488C>T| |
S186 |
| 15462 | BAA01g11860 | A01 | 5544960 | C | T | downstream_gene_variant | MODIFIER | c.*2001G>A| |
S115 |
| 15463 | BAA01g11850 | A01 | 5545446 | C | T | downstream_gene_variant | MODIFIER | c.*319C>T| |
S158 |
| 15464 | BAA01g11850 | A01 | 5546403 | C | T | downstream_gene_variant | MODIFIER | c.*1276C>T| |
S239 |
| 15465 | BAA01g11850 | A01 | 5546550 | T | A | downstream_gene_variant | MODIFIER | c.*1423T>A| |
S177 |
| 15466 | BAA01g11850 | A01 | 5546948 | C | T | downstream_gene_variant | MODIFIER | c.*1821C>T| |
S302 |
| 15467 | BAA01g11860 | A01 | 5547032 | C | T | missense_variant | MODERATE | c.865G>A|p.Glu289Lys |
S268 |
| 15468 | BAA01g11860 | A01 | 5549040 | G | A | upstream_gene_variant | MODIFIER | c.-194C>T| |
S293 |
| 15469 | BAA01g11860 | A01 | 5550090 | G | A | upstream_gene_variant | MODIFIER | c.-1244C>T| |
S144 |
| 15470 | BAA01g11870 | A01 | 5553591 | C | T | synonymous_variant | LOW | c.4866G>A|p.Val1622Val |
S18 |
| 15471 | BAA01g11870 | A01 | 5553729 | G | A | synonymous_variant | LOW | c.4728C>T|p.Arg1576Arg |
S138 |
| 15472 | BAA01g11870 | A01 | 5553990 | G | A | synonymous_variant | LOW | c.4467C>T|p.Arg1489Arg |
S165 |
| 15473 | BAA01g11870 | A01 | 5554272 | G | A | synonymous_variant | LOW | c.4185C>T|p.Leu1395Leu |
S201 |
| 15474 | BAA01g11870 | A01 | 5554613 | C | T | missense_variant | MODERATE | c.3844G>A|p.Ala1282Thr |
S167 |
| 15475 | BAA01g11870 | A01 | 5554932 | C | T | missense_variant | MODERATE | c.3525G>A|p.Met1175Ile |
S18 |