| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g22870 | A10 | 19461165 | A | G | missense_variant | MODERATE | c.1262T>C|p.Phe421Ser |
S13 |
| 2 | BAA10g22870 | A10 | 19461431 | C | T | splice_region_variant&intron_variant | LOW | c.1176+5G>A| |
S135 |
| 3 | BAA10g22870 | A10 | 19461681 | C | T | missense_variant | MODERATE | c.1022G>A|p.Cys341Tyr |
S107 |
| 4 | BAA10g22870 | A10 | 19463200 | C | T | splice_region_variant&intron_variant | LOW | c.308+4G>A| |
S96 |
| 5 | BAA10g22870 | A10 | 19463469 | G | A | missense_variant | MODERATE | c.127C>T|p.Pro43Ser |
S32 |
| 6 | BAA10g22870 | A10 | 19464692 | G | A | upstream_gene_variant | MODIFIER | c.-979C>T| |
S63 |
| 7 | BAA10g22870 | A10 | 19466304 | C | T | upstream_gene_variant | MODIFIER | c.-2591G>A| |
S10 |
| 8 | BAA10g22870 | A10 | 19467159 | C | T | upstream_gene_variant | MODIFIER | c.-3446G>A| |
S188 |