| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00970 | A10 | 460695 | C | T | downstream_gene_variant | MODIFIER | c.*4378G>A| |
S308 |
| 2 | BAA10g00970 | A10 | 465111 | G | A | synonymous_variant | LOW | c.1099C>T|p.Leu367Leu |
S18 |
| 3 | BAA10g00970 | A10 | 465755 | C | T | missense_variant | MODERATE | c.634G>A|p.Asp212Asn |
S238 |
| 4 | BAA10g00970 | A10 | 466354 | C | T | missense_variant | MODERATE | c.199G>A|p.Gly67Ser |
S281 |
| 5 | BAA10g00970 | A10 | 466864 | C | T | upstream_gene_variant | MODIFIER | c.-245G>A| |
S67 |
| 6 | BAA10g00970 | A10 | 468911 | G | A | upstream_gene_variant | MODIFIER | c.-2292C>T| |
S100 |
| 7 | BAA10g00970 | A10 | 469666 | G | A | upstream_gene_variant | MODIFIER | c.-3047C>T| |
S80 |