| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 79451 | BAA01g41800 | A01 | 27811040 | C | T | upstream_gene_variant | MODIFIER | c.-2667C>T| |
S109 |
| 79452 | BAA01g41790 | A01 | 27811333 | G | A | missense_variant | MODERATE | c.1075G>A|p.Glu359Lys |
S299 |
| 79453 | BAA01g41790 | A01 | 27811420 | G | A | missense_variant | MODERATE | c.1162G>A|p.Glu388Lys |
S122 |
| 79454 | BAA01g41800 | A01 | 27812083 | G | A | upstream_gene_variant | MODIFIER | c.-1624G>A| |
S5 |
| 79455 | BAA01g41800 | A01 | 27812619 | C | T | upstream_gene_variant | MODIFIER | c.-1088C>T| |
S266 |
| 79456 | BAA01g41800 | A01 | 27812913 | G | A | upstream_gene_variant | MODIFIER | c.-794G>A| |
S51 |
| 79457 | BAA01g41800 | A01 | 27813016 | C | T | upstream_gene_variant | MODIFIER | c.-691C>T| |
S251 |
| 79458 | BAA01g41800 | A01 | 27814377 | C | T | synonymous_variant | LOW | c.513C>T|p.Tyr171Tyr |
S192 |
| 79459 | BAA01g41800 | A01 | 27814494 | C | T | synonymous_variant | LOW | c.630C>T|p.Leu210Leu |
S275 |
| 79460 | BAA01g41800 | A01 | 27814582 | C | T | missense_variant | MODERATE | c.718C>T|p.Pro240Ser |
S162 |
| 79461 | BAA01g41790 | A01 | 27815231 | G | A | downstream_gene_variant | MODIFIER | c.*3515G>A| |
S197 |
| 79462 | BAA01g41790 | A01 | 27815994 | C | T | downstream_gene_variant | MODIFIER | c.*4278C>T| |
S54 |
| 79463 | BAA01g41800 | A01 | 27817007 | G | A | downstream_gene_variant | MODIFIER | c.*2357G>A| |
S271 |
| 79464 | BAA01g41800 | A01 | 27817044 | C | T | downstream_gene_variant | MODIFIER | c.*2394C>T| |
S26 |
| 79465 | BAA01g41800 | A01 | 27817169 | C | T | downstream_gene_variant | MODIFIER | c.*2519C>T| |
S130 |
| 79466 | BAA01g41810 | A01 | 27817316 | C | T | missense_variant | MODERATE | c.3629G>A|p.Arg1210Lys |
S192 |
| 79467 | BAA01g41810 | A01 | 27817363 | C | T | synonymous_variant | LOW | c.3582G>A|p.Glu1194Glu |
S269 |
| 79468 | BAA01g41810 | A01 | 27817992 | C | T | missense_variant | MODERATE | c.3067G>A|p.Ala1023Thr |
S133 |
| 79469 | BAA01g41810 | A01 | 27818914 | C | T | missense_variant | MODERATE | c.2261G>A|p.Gly754Glu |
S266 |
| 79470 | BAA01g41810 | A01 | 27819348 | A | G | synonymous_variant | LOW | c.1827T>C|p.Asn609Asn |
S255 |
| 79471 | BAA01g41810 | A01 | 27819414 | C | T | synonymous_variant | LOW | c.1761G>A|p.Leu587Leu |
S10 |
| 79472 | BAA01g41810 | A01 | 27820053 | C | T | missense_variant | MODERATE | c.1122G>A|p.Met374Ile |
S198 |
| 79473 | BAA01g41810 | A01 | 27820895 | C | T | missense_variant | MODERATE | c.280G>A|p.Glu94Lys |
S158 |
| 79474 | BAA01g41810 | A01 | 27821166 | G | A | synonymous_variant | LOW | c.9C>T|p.Leu3Leu |
S252 |
| 79475 | BAA01g41810 | A01 | 27821524 | G | A | upstream_gene_variant | MODIFIER | c.-350C>T| |
S252 |