| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g01440 | A08 | 1055620 | C | T | upstream_gene_variant | MODIFIER | c.-4587C>T| |
S291 |
| 2 | BAA08g01440 | A08 | 1059132 | G | A | upstream_gene_variant | MODIFIER | c.-1075G>A| |
S234 |
| 3 | BAA08g01440 | A08 | 1059638 | C | T | upstream_gene_variant | MODIFIER | c.-569C>T| |
S209 |
| 4 | BAA08g01440 | A08 | 1059923 | G | A | upstream_gene_variant | MODIFIER | c.-284G>A| |
S87 |
| 5 | BAA08g01440 | A08 | 1059990 | C | T | upstream_gene_variant | MODIFIER | c.-217C>T| |
S230 |
| 6 | BAA08g01440 | A08 | 1060289 | C | T | missense_variant | MODERATE | c.83C>T|p.Ser28Phe |
S153 S213 |
| 7 | BAA08g01440 | A08 | 1061408 | C | T | missense_variant | MODERATE | c.1202C>T|p.Ser401Phe |
S280 |
| 8 | BAA08g01440 | A08 | 1063214 | G | A | downstream_gene_variant | MODIFIER | c.*1790G>A| |
S38 |
| 9 | BAA08g01440 | A08 | 1063523 | C | T | downstream_gene_variant | MODIFIER | c.*2099C>T| |
S12 S62 |
| 10 | BAA08g01440 | A08 | 1063624 | C | T | downstream_gene_variant | MODIFIER | c.*2200C>T| |
|
| 11 | BAA08g01440 | A08 | 1064226 | C | T | downstream_gene_variant | MODIFIER | c.*2802C>T| |
S289 S290 |
| 12 | BAA08g01440 | A08 | 1064995 | C | T | downstream_gene_variant | MODIFIER | c.*3571C>T| |
S186 S275 |