| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g16870 | A10 | 16498997 | C | T | upstream_gene_variant | MODIFIER | c.-4621C>T| |
S150 |
| 2 | BAA10g16870 | A10 | 16501293 | G | A | upstream_gene_variant | MODIFIER | c.-2325G>A| |
S234 |
| 3 | BAA10g16870 | A10 | 16501436 | G | A | upstream_gene_variant | MODIFIER | c.-2182G>A| |
S148 S210 S30 S31 |
| 4 | BAA10g16870 | A10 | 16501490 | C | T | upstream_gene_variant | MODIFIER | c.-2128C>T| |
S123 |
| 5 | BAA10g16870 | A10 | 16502421 | C | T | upstream_gene_variant | MODIFIER | c.-1197C>T| |
S162 |
| 6 | BAA10g16870 | A10 | 16503818 | G | A | synonymous_variant | LOW | c.201G>A|p.Gln67Gln |
S57 |
| 7 | BAA10g16870 | A10 | 16504327 | C | T | missense_variant | MODERATE | c.620C>T|p.Ala207Val |
S68 |
| 8 | BAA10g16870 | A10 | 16504941 | G | A | missense_variant | MODERATE | c.844G>A|p.Asp282Asn |
S36 |