| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 50951 | BAA01g28490 | A01 | 17567574 | C | T | upstream_gene_variant | MODIFIER | c.-2427G>A| |
S130 |
| 50952 | BAA01g28490 | A01 | 17567582 | G | A | upstream_gene_variant | MODIFIER | c.-2435C>T| |
S288 |
| 50953 | BAA01g28490 | A01 | 17567705 | C | T | upstream_gene_variant | MODIFIER | c.-2558G>A| |
S181 S56 |
| 50954 | BAA01g28490 | A01 | 17568138 | C | T | upstream_gene_variant | MODIFIER | c.-2991G>A| |
S128 |
| 50955 | BAA01g28490 | A01 | 17568152 | G | A | upstream_gene_variant | MODIFIER | c.-3005C>T| |
S280 |
| 50956 | BAA01g28490 | A01 | 17568282 | C | T | upstream_gene_variant | MODIFIER | c.-3135G>A| |
S10 |
| 50957 | BAA01g28490 | A01 | 17568702 | G | A | upstream_gene_variant | MODIFIER | c.-3555C>T| |
S100 |
| 50958 | BAA01g28490 | A01 | 17568926 | G | A | upstream_gene_variant | MODIFIER | c.-3779C>T| |
S122 |
| 50959 | BAA01g28490 | A01 | 17569079 | C | T | upstream_gene_variant | MODIFIER | c.-3932G>A| |
S282 |
| 50960 | BAA01g28490 | A01 | 17569158 | C | T | upstream_gene_variant | MODIFIER | c.-4011G>A| |
S200 |
| 50961 | BAA01g28490 | A01 | 17569817 | G | A | upstream_gene_variant | MODIFIER | c.-4670C>T| |
S62 |
| 50962 | BAA01g28490-BAA01g28500 | A01 | 17570887 | C | T | intergenic_region | MODIFIER | n.17570887C>T| |
S166 |
| 50963 | BAA01g28500 | A01 | 17581159 | C | T | downstream_gene_variant | MODIFIER | c.*2520G>A| |
S170 |
| 50964 | BAA01g28500 | A01 | 17583133 | G | A | downstream_gene_variant | MODIFIER | c.*546C>T| |
S149 |
| 50965 | BAA01g28510 | A01 | 17584140 | C | T | upstream_gene_variant | MODIFIER | c.-4128C>T| |
S20 |
| 50966 | BAA01g28500 | A01 | 17585174 | C | T | synonymous_variant | LOW | c.1692G>A|p.Leu564Leu |
S56 |
| 50967 | BAA01g28510 | A01 | 17585249 | G | A | upstream_gene_variant | MODIFIER | c.-3019G>A| |
S172 S217 |
| 50968 | BAA01g28500 | A01 | 17585368 | G | A | missense_variant | MODERATE | c.1571C>T|p.Pro524Leu |
S116 |
| 50969 | BAA01g28500 | A01 | 17585437 | G | A | missense_variant | MODERATE | c.1502C>T|p.Ala501Val |
S155 S211 |
| 50970 | BAA01g28510 | A01 | 17585798 | G | A | upstream_gene_variant | MODIFIER | c.-2470G>A| |
S138 |
| 50971 | BAA01g28500 | A01 | 17586687 | C | T | splice_donor_variant&intron_variant | HIGH | c.679+1G>A| |
S293 |
| 50972 | BAA01g28500 | A01 | 17586717 | G | A | missense_variant | MODERATE | c.650C>T|p.Pro217Leu |
S114 |
| 50973 | BAA01g28500 | A01 | 17587204 | C | T | missense_variant | MODERATE | c.355G>A|p.Ala119Thr |
S42 |
| 50974 | BAA01g28510 | A01 | 17588614 | G | A | missense_variant | MODERATE | c.347G>A|p.Gly116Glu |
S67 |
| 50975 | BAA01g28510 | A01 | 17589096 | G | A | missense_variant | MODERATE | c.559G>A|p.Gly187Arg |
S241 |