| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g39050 | A09 | 46775866 | C | T | upstream_gene_variant | MODIFIER | c.-4823C>T| |
S277 |
| 2 | BAA09g39050 | A09 | 46775991 | G | A | upstream_gene_variant | MODIFIER | c.-4698G>A| |
S53 |
| 3 | BAA09g39050 | A09 | 46776355 | C | T | upstream_gene_variant | MODIFIER | c.-4334C>T| |
S183 S198 |
| 4 | BAA09g39050 | A09 | 46776514 | G | A | upstream_gene_variant | MODIFIER | c.-4175G>A| |
S249 |
| 5 | BAA09g39050 | A09 | 46777037 | G | A | upstream_gene_variant | MODIFIER | c.-3652G>A| |
S65 |
| 6 | BAA09g39050 | A09 | 46777406 | C | T | upstream_gene_variant | MODIFIER | c.-3283C>T| |
S37 |
| 7 | BAA09g39050 | A09 | 46778095 | G | A | upstream_gene_variant | MODIFIER | c.-2594G>A| |
S246 |
| 8 | BAA09g39050 | A09 | 46778799 | C | T | upstream_gene_variant | MODIFIER | c.-1890C>T| |
S64 |
| 9 | BAA09g39050 | A09 | 46778863 | G | A | upstream_gene_variant | MODIFIER | c.-1826G>A| |
S62 |
| 10 | BAA09g39050 | A09 | 46779093 | G | A | upstream_gene_variant | MODIFIER | c.-1596G>A| |
S150 |
| 11 | BAA09g39050 | A09 | 46779096 | G | A | upstream_gene_variant | MODIFIER | c.-1593G>A| |
S244 |
| 12 | BAA09g39050 | A09 | 46779310 | C | T | upstream_gene_variant | MODIFIER | c.-1379C>T| |
S108 S290 |
| 13 | BAA09g39050 | A09 | 46779541 | G | A | upstream_gene_variant | MODIFIER | c.-1148G>A| |
S199 |
| 14 | BAA09g39050 | A09 | 46779903 | C | T | upstream_gene_variant | MODIFIER | c.-786C>T| |
S306 S308 |
| 15 | BAA09g39050 | A09 | 46779986 | C | T | upstream_gene_variant | MODIFIER | c.-703C>T| |
S37 |
| 16 | BAA09g39050 | A09 | 46780454 | G | A | upstream_gene_variant | MODIFIER | c.-235G>A| |
S189 |
| 17 | BAA09g39050 | A09 | 46780480 | G | A | upstream_gene_variant | MODIFIER | c.-209G>A| |
S15 S3 |
| 18 | BAA09g39050 | A09 | 46780740 | C | T | missense_variant | MODERATE | c.52C>T|p.Leu18Phe |
S228 |
| 19 | BAA09g39050 | A09 | 46781090 | C | T | synonymous_variant | LOW | c.282C>T|p.Leu94Leu |
S280 |
| 20 | BAA09g39050 | A09 | 46781097 | G | A | missense_variant | MODERATE | c.289G>A|p.Asp97Asn |
S204 |
| 21 | BAA09g39050 | A09 | 46782611 | T | C | downstream_gene_variant | MODIFIER | c.*1479T>C| |
S217 |
| 22 | BAA09g39050 | A09 | 46783539 | C | T | downstream_gene_variant | MODIFIER | c.*2407C>T| |
S269 |
| 23 | BAA09g39050 | A09 | 46783601 | C | T | downstream_gene_variant | MODIFIER | c.*2469C>T| |
S210 |
| 24 | BAA09g39050 | A09 | 46784048 | G | A | downstream_gene_variant | MODIFIER | c.*2916G>A| |
S274 |
| 25 | BAA09g39050 | A09 | 46784887 | C | T | downstream_gene_variant | MODIFIER | c.*3755C>T| |
S302 |