| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g01630 | A10 | 790901 | G | A | downstream_gene_variant | MODIFIER | c.*2277C>T| |
S66 |
| 2 | BAA10g01630 | A10 | 791668 | C | T | downstream_gene_variant | MODIFIER | c.*1510G>A| |
S104 S52 |
| 3 | BAA10g01630 | A10 | 791736 | C | T | downstream_gene_variant | MODIFIER | c.*1442G>A| |
S275 |
| 4 | BAA10g01630 | A10 | 792355 | G | A | downstream_gene_variant | MODIFIER | c.*823C>T| |
S276 |
| 5 | BAA10g01630 | A10 | 793636 | C | T | missense_variant | MODERATE | c.439G>A|p.Gly147Arg |
S44 |
| 6 | BAA10g01630 | A10 | 794592 | C | T | missense_variant&splice_region_variant | MODERATE | c.139G>A|p.Ala47Thr |
S110 |
| 7 | BAA10g01630 | A10 | 794847 | C | T | upstream_gene_variant | MODIFIER | c.-117G>A| |
S150 |
| 8 | BAA10g01630 | A10 | 795200 | G | A | upstream_gene_variant | MODIFIER | c.-470C>T| |
S80 |
| 9 | BAA10g01630 | A10 | 798585 | G | A | upstream_gene_variant | MODIFIER | c.-3855C>T| |
S216 |