| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 24801 | BAA01g17920 | A01 | 8727843 | G | A | downstream_gene_variant | MODIFIER | c.*4311G>A| |
S168 |
| 24802 | BAA01g17920 | A01 | 8727949 | C | T | downstream_gene_variant | MODIFIER | c.*4417C>T| |
S18 |
| 24803 | BAA01g17920 | A01 | 8727965 | C | T | downstream_gene_variant | MODIFIER | c.*4433C>T| |
S70 |
| 24804 | BAA01g17920 | A01 | 8728070 | G | A | downstream_gene_variant | MODIFIER | c.*4538G>A| |
S306 |
| 24805 | BAA01g17920 | A01 | 8728103 | G | A | downstream_gene_variant | MODIFIER | c.*4571G>A| |
S187 |
| 24806 | BAA01g17920 | A01 | 8728111 | G | A | downstream_gene_variant | MODIFIER | c.*4579G>A| |
S37 |
| 24807 | BAA01g17920 | A01 | 8728248 | G | A | downstream_gene_variant | MODIFIER | c.*4716G>A| |
S187 |
| 24808 | BAA01g17920 | A01 | 8728297 | C | T | downstream_gene_variant | MODIFIER | c.*4765C>T| |
S69 |
| 24809 | BAA01g17920 | A01 | 8728318 | C | T | downstream_gene_variant | MODIFIER | c.*4786C>T| |
S112 |
| 24810 | BAA01g17930 | A01 | 8731489 | C | T | upstream_gene_variant | MODIFIER | c.-41G>A| |
S135 |
| 24811 | BAA01g17930 | A01 | 8733161 | C | T | upstream_gene_variant | MODIFIER | c.-1713G>A| |
S40 S49 |
| 24812 | BAA01g17930 | A01 | 8734485 | G | A | upstream_gene_variant | MODIFIER | c.-3037C>T| |
S203 |
| 24813 | BAA01g17930 | A01 | 8734852 | G | A | upstream_gene_variant | MODIFIER | c.-3404C>T| |
S156 |
| 24814 | BAA01g17930 | A01 | 8735094 | G | A | upstream_gene_variant | MODIFIER | c.-3646C>T| |
S8 |
| 24815 | BAA01g17930 | A01 | 8736104 | G | A | upstream_gene_variant | MODIFIER | c.-4656C>T| |
S67 |
| 24816 | BAA01g17940 | A01 | 8736301 | G | A | synonymous_variant | LOW | c.57G>A|p.Lys19Lys |
S217 S248 |
| 24817 | BAA01g17940 | A01 | 8736439 | G | A | missense_variant&splice_region_variant | MODERATE | c.89G>A|p.Gly30Asp |
S297 |
| 24818 | BAA01g17940 | A01 | 8736481 | C | T | missense_variant | MODERATE | c.131C>T|p.Ala44Val |
S265 |
| 24819 | BAA01g17940 | A01 | 8736612 | G | A | missense_variant&splice_region_variant | MODERATE | c.187G>A|p.Asp63Asn |
S251 |
| 24820 | BAA01g17940 | A01 | 8740866 | C | T | intron_variant | MODIFIER | c.1533+1037C>T| |
S112 |
| 24821 | BAA01g17940 | A01 | 8741482 | C | T | intron_variant | MODIFIER | c.1533+1653C>T| |
S18 |
| 24822 | BAA01g17940 | A01 | 8741700 | G | A | intron_variant | MODIFIER | c.1533+1871G>A| |
S59 |
| 24823 | BAA01g17940 | A01 | 8741859 | C | T | intron_variant | MODIFIER | c.1533+2030C>T| |
S160 |
| 24824 | BAA01g17940 | A01 | 8742299 | C | T | intron_variant | MODIFIER | c.1533+2470C>T| |
S107 |
| 24825 | BAA01g17940 | A01 | 8742959 | G | A | intron_variant | MODIFIER | c.1533+3130G>A| |
S122 |