| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g06470 | A08 | 5224439 | C | T | upstream_gene_variant | MODIFIER | c.-4106C>T| |
S235 |
| 2 | BAA08g06470 | A08 | 5224518 | C | T | upstream_gene_variant | MODIFIER | c.-4027C>T| |
S292 |
| 3 | BAA08g06470 | A08 | 5224957 | G | A | upstream_gene_variant | MODIFIER | c.-3588G>A| |
S274 |
| 4 | BAA08g06470 | A08 | 5226904 | C | T | upstream_gene_variant | MODIFIER | c.-1641C>T| |
S112 |
| 5 | BAA08g06470 | A08 | 5227275 | C | T | upstream_gene_variant | MODIFIER | c.-1270C>T| |
S60 |
| 6 | BAA08g06470 | A08 | 5227285 | G | A | upstream_gene_variant | MODIFIER | c.-1260G>A| |
S78 |
| 7 | BAA08g06470 | A08 | 5227811 | G | A | upstream_gene_variant | MODIFIER | c.-734G>A| |
S32 |
| 8 | BAA08g06470 | A08 | 5227890 | C | T | upstream_gene_variant | MODIFIER | c.-655C>T| |
S157 S163 |
| 9 | BAA08g06470 | A08 | 5227932 | G | A | upstream_gene_variant | MODIFIER | c.-613G>A| |
S229 |
| 10 | BAA08g06470 | A08 | 5228474 | C | T | upstream_gene_variant | MODIFIER | c.-71C>T| |
S169 |
| 11 | BAA08g06470 | A08 | 5228620 | G | A | intron_variant | MODIFIER | c.51+25G>A| |
S124 |
| 12 | BAA08g06470 | A08 | 5228660 | C | T | splice_region_variant&intron_variant | LOW | c.52-7C>T| |
S203 |
| 13 | BAA08g06470 | A08 | 5228838 | G | A | intron_variant | MODIFIER | c.172-14G>A| |
S157 |
| 14 | BAA08g06470 | A08 | 5228900 | G | A | missense_variant | MODERATE | c.220G>A|p.Glu74Lys |
S84 |
| 15 | BAA08g06470 | A08 | 5230449 | C | T | intron_variant | MODIFIER | c.980+13C>T| |
S206 S26 |
| 16 | BAA08g06470 | A08 | 5231337 | G | A | missense_variant | MODERATE | c.1225G>A|p.Asp409Asn |
S33 |
| 17 | BAA08g06470 | A08 | 5231434 | G | A | missense_variant | MODERATE | c.1322G>A|p.Gly441Asp |
S275 |