| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 128951 | BAA10g16950-BAA10g16960 | A10 | 16539688 | G | A | intergenic_region | MODIFIER | n.16539688G>A| |
S255 |
| 128952 | BAA10g16950-BAA10g16960 | A10 | 16540019 | T | A | intergenic_region | MODIFIER | n.16540019T>A| |
S33 |
| 128953 | BAA10g16950-BAA10g16960 | A10 | 16540274 | G | A | intergenic_region | MODIFIER | n.16540274G>A| |
S50 |
| 128954 | BAA10g16970 | A10 | 16549559 | C | T | upstream_gene_variant | MODIFIER | c.-2187C>T| |
S169 S173 S225 |
| 128955 | BAA10g16970 | A10 | 16550383 | G | A | upstream_gene_variant | MODIFIER | c.-1363G>A| |
S294 |
| 128956 | BAA10g16970 | A10 | 16550541 | C | T | upstream_gene_variant | MODIFIER | c.-1205C>T| |
S124 |
| 128957 | BAA10g16970 | A10 | 16550714 | G | A | upstream_gene_variant | MODIFIER | c.-1032G>A| |
S280 |
| 128958 | BAA10g16970 | A10 | 16551050 | C | T | upstream_gene_variant | MODIFIER | c.-696C>T| |
S153 S213 |
| 128959 | BAA10g16980 | A10 | 16552904 | G | A | upstream_gene_variant | MODIFIER | c.-2236G>A| |
S34 |
| 128960 | BAA10g16980 | A10 | 16553020 | G | A | upstream_gene_variant | MODIFIER | c.-2120G>A| |
S132 S137 S215 |
| 128961 | BAA10g16980 | A10 | 16554349 | G | A | upstream_gene_variant | MODIFIER | c.-791G>A| |
S255 |
| 128962 | BAA10g16990 | A10 | 16556540 | G | A | upstream_gene_variant | MODIFIER | c.-4296G>A| |
S174 S27 |
| 128963 | BAA10g16990 | A10 | 16556933 | G | A | upstream_gene_variant | MODIFIER | c.-3903G>A| |
S217 |
| 128964 | BAA10g16990 | A10 | 16558616 | C | T | upstream_gene_variant | MODIFIER | c.-2220C>T| |
S299 |
| 128965 | BAA10g16990 | A10 | 16558983 | C | T | upstream_gene_variant | MODIFIER | c.-1853C>T| |
S249 |
| 128966 | BAA10g16990 | A10 | 16560201 | G | A | upstream_gene_variant | MODIFIER | c.-635G>A| |
S155 S211 |
| 128967 | BAA10g16990 | A10 | 16561625 | G | A | missense_variant | MODERATE | c.533G>A|p.Arg178Lys |
S158 |
| 128968 | BAA10g16990 | A10 | 16561840 | C | T | intron_variant | MODIFIER | c.649+99C>T| |
S19 |
| 128969 | BAA10g16990 | A10 | 16562704 | G | A | intron_variant | MODIFIER | c.650-446G>A| |
S178 |
| 128970 | BAA10g16990 | A10 | 16565644 | G | A | downstream_gene_variant | MODIFIER | c.*2009G>A| |
S67 |
| 128971 | BAA10g16990 | A10 | 16566361 | C | T | downstream_gene_variant | MODIFIER | c.*2726C>T| |
S282 |
| 128972 | BAA10g16990 | A10 | 16566694 | G | A | downstream_gene_variant | MODIFIER | c.*3059G>A| |
S132 S215 S89 |
| 128973 | BAA10g16990 | A10 | 16568003 | C | T | downstream_gene_variant | MODIFIER | c.*4368C>T| |
S177 |
| 128974 | BAA10g16990 | A10 | 16568176 | C | T | downstream_gene_variant | MODIFIER | c.*4541C>T| |
S47 |
| 128975 | BAA10g16990-BAA10g17000 | A10 | 16569492 | C | T | intergenic_region | MODIFIER | n.16569492C>T| |
S149 |