| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 16401 | BAA01g12430 | A01 | 5861077 | C | T | upstream_gene_variant | MODIFIER | c.-3714C>T| |
S7 |
| 16402 | BAA01g12430 | A01 | 5861114 | G | A | upstream_gene_variant | MODIFIER | c.-3677G>A| |
S149 |
| 16403 | BAA01g12430 | A01 | 5861269 | C | T | upstream_gene_variant | MODIFIER | c.-3522C>T| |
S213 |
| 16404 | BAA01g12430 | A01 | 5863313 | G | A | upstream_gene_variant | MODIFIER | c.-1478G>A| |
S294 |
| 16405 | BAA01g12430 | A01 | 5865514 | G | A | missense_variant | MODERATE | c.724G>A|p.Gly242Arg |
S234 |
| 16406 | BAA01g12430 | A01 | 5866070 | G | A | missense_variant | MODERATE | c.1280G>A|p.Gly427Glu |
S86 |
| 16407 | BAA01g12430 | A01 | 5866218 | C | T | synonymous_variant | LOW | c.1428C>T|p.Phe476Phe |
S247 |
| 16408 | BAA01g12430 | A01 | 5866375 | C | T | missense_variant | MODERATE | c.1585C>T|p.Pro529Ser |
S100 |
| 16409 | BAA01g12430 | A01 | 5866392 | G | A | synonymous_variant | LOW | c.1602G>A|p.Gln534Gln |
S298 |
| 16410 | BAA01g12430 | A01 | 5866622 | C | T | missense_variant | MODERATE | c.1832C>T|p.Ser611Phe |
S146 |
| 16411 | BAA01g12430 | A01 | 5867093 | G | A | missense_variant | MODERATE | c.2303G>A|p.Gly768Glu |
S92 |
| 16412 | BAA01g12430 | A01 | 5867784 | G | A | missense_variant | MODERATE | c.2638G>A|p.Glu880Lys |
S272 |
| 16413 | BAA01g12440 | A01 | 5868089 | G | A | upstream_gene_variant | MODIFIER | c.-2972G>A| |
S28 |
| 16414 | BAA01g12440 | A01 | 5868924 | C | T | upstream_gene_variant | MODIFIER | c.-2137C>T| |
S61 |
| 16415 | BAA01g12440 | A01 | 5868941 | C | T | upstream_gene_variant | MODIFIER | c.-2120C>T| |
S286 |
| 16416 | BAA01g12440 | A01 | 5869151 | C | T | upstream_gene_variant | MODIFIER | c.-1910C>T| |
S182 |
| 16417 | BAA01g12440 | A01 | 5869955 | C | T | upstream_gene_variant | MODIFIER | c.-1106C>T| |
S270 |
| 16418 | BAA01g12440 | A01 | 5870057 | G | A | upstream_gene_variant | MODIFIER | c.-1004G>A| |
S272 |
| 16419 | BAA01g12440 | A01 | 5870575 | G | A | upstream_gene_variant | MODIFIER | c.-486G>A| |
S272 |
| 16420 | BAA01g12440 | A01 | 5871174 | G | A | synonymous_variant | LOW | c.114G>A|p.Gln38Gln |
S149 |
| 16421 | BAA01g12440 | A01 | 5871236 | C | T | missense_variant | MODERATE | c.176C>T|p.Ser59Phe |
S4 |
| 16422 | BAA01g12440 | A01 | 5871265 | G | A | missense_variant | MODERATE | c.205G>A|p.Asp69Asn |
S17 |
| 16423 | BAA01g12440 | A01 | 5871787 | G | A | missense_variant | MODERATE | c.500G>A|p.Gly167Glu |
S60 |
| 16424 | BAA01g12440 | A01 | 5873831 | G | A | downstream_gene_variant | MODIFIER | c.*1932G>A| |
S195 |
| 16425 | BAA01g12450 | A01 | 5874209 | C | T | missense_variant | MODERATE | c.365C>T|p.Ser122Phe |
S79 S84 |