| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g15930 | A10 | 16053101 | C | T | upstream_gene_variant | MODIFIER | c.-4331C>T| |
S191 |
| 2 | BAA10g15930 | A10 | 16054646 | G | A | upstream_gene_variant | MODIFIER | c.-2786G>A| |
S139 |
| 3 | BAA10g15930 | A10 | 16056085 | G | A | upstream_gene_variant | MODIFIER | c.-1347G>A| |
S293 |
| 4 | BAA10g15930 | A10 | 16056224 | C | T | upstream_gene_variant | MODIFIER | c.-1208C>T| |
S283 |
| 5 | BAA10g15930 | A10 | 16056240 | C | T | upstream_gene_variant | MODIFIER | c.-1192C>T| |
S146 |
| 6 | BAA10g15930 | A10 | 16057533 | C | T | synonymous_variant | LOW | c.102C>T|p.Leu34Leu |
S277 |
| 7 | BAA10g15930 | A10 | 16057554 | G | A | synonymous_variant | LOW | c.123G>A|p.Glu41Glu |
S9 |
| 8 | BAA10g15930 | A10 | 16058569 | C | T | missense_variant | MODERATE | c.847C>T|p.Pro283Ser |
S294 |
| 9 | BAA10g15930 | A10 | 16058980 | G | A | missense_variant | MODERATE | c.1069G>A|p.Glu357Lys |
S182 |
| 10 | BAA10g15930 | A10 | 16059046 | G | A | missense_variant | MODERATE | c.1135G>A|p.Asp379Asn |
S251 |