| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 184551 | BAA02g22650 | A02 | 12280087 | C | T | missense_variant | MODERATE | c.1283C>T|p.Thr428Ile |
S219 S72 |
| 184552 | BAA02g22650 | A02 | 12280203 | G | A | missense_variant | MODERATE | c.1399G>A|p.Ala467Thr |
S45 |
| 184553 | BAA02g22650 | A02 | 12280486 | C | T | downstream_gene_variant | MODIFIER | c.*4C>T| |
S296 |
| 184554 | BAA02g22650 | A02 | 12280860 | G | A | downstream_gene_variant | MODIFIER | c.*378G>A| |
S207 |
| 184555 | BAA02g22660 | A02 | 12283372 | G | A | missense_variant | MODERATE | c.205C>T|p.Pro69Ser |
S45 |
| 184556 | BAA02g22660 | A02 | 12283537 | C | T | missense_variant | MODERATE | c.40G>A|p.Val14Met |
S170 |
| 184557 | BAA02g22660 | A02 | 12283544 | C | T | synonymous_variant | LOW | c.33G>A|p.Gln11Gln |
S85 |
| 184558 | BAA02g22660 | A02 | 12286164 | G | A | upstream_gene_variant | MODIFIER | c.-2588C>T| |
S17 |
| 184559 | BAA02g22660 | A02 | 12286189 | G | A | upstream_gene_variant | MODIFIER | c.-2613C>T| |
S37 |
| 184560 | BAA02g22660 | A02 | 12286594 | G | A | upstream_gene_variant | MODIFIER | c.-3018C>T| |
S72 S78 |
| 184561 | BAA02g22660 | A02 | 12286720 | C | T | upstream_gene_variant | MODIFIER | c.-3144G>A| |
S305 |
| 184562 | BAA02g22660 | A02 | 12287197 | C | T | upstream_gene_variant | MODIFIER | c.-3621G>A| |
S65 |
| 184563 | BAA02g22660 | A02 | 12287200 | C | T | upstream_gene_variant | MODIFIER | c.-3624G>A| |
S255 |
| 184564 | BAA02g22670 | A02 | 12289035 | C | T | downstream_gene_variant | MODIFIER | c.*2532G>A| |
S261 |
| 184565 | BAA02g22670 | A02 | 12289042 | C | T | downstream_gene_variant | MODIFIER | c.*2525G>A| |
S255 |
| 184566 | BAA02g22670 | A02 | 12291643 | C | T | missense_variant | MODERATE | c.3158G>A|p.Arg1053Lys |
S127 |
| 184567 | BAA02g22670 | A02 | 12291773 | G | A | missense_variant | MODERATE | c.3028C>T|p.His1010Tyr |
S263 |
| 184568 | BAA02g22670 | A02 | 12292226 | C | T | missense_variant | MODERATE | c.2575G>A|p.Gly859Ser |
S289 S290 |
| 184569 | BAA02g22670 | A02 | 12292253 | C | T | missense_variant | MODERATE | c.2548G>A|p.Asp850Asn |
S18 |
| 184570 | BAA02g22670 | A02 | 12293501 | G | A | missense_variant | MODERATE | c.1300C>T|p.Leu434Phe |
S45 |
| 184571 | BAA02g22670 | A02 | 12294462 | G | A | synonymous_variant | LOW | c.339C>T|p.Asn113Asn |
S133 |
| 184572 | BAA02g22670 | A02 | 12294660 | G | A | synonymous_variant | LOW | c.141C>T|p.Ser47Ser |
S50 |
| 184573 | BAA02g22670 | A02 | 12295066 | C | T | upstream_gene_variant | MODIFIER | c.-266G>A| |
S296 |
| 184574 | BAA02g22670 | A02 | 12295591 | C | T | upstream_gene_variant | MODIFIER | c.-791G>A| |
S277 |
| 184575 | BAA02g22670 | A02 | 12296254 | G | A | upstream_gene_variant | MODIFIER | c.-1454C>T| |
S7 |