| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g21950 | A10 | 19112882 | C | T | upstream_gene_variant | MODIFIER | c.-2000C>T| |
S168 |
| 2 | BAA10g21950 | A10 | 19113600 | G | A | upstream_gene_variant | MODIFIER | c.-1282G>A| |
S294 |
| 3 | BAA10g21950 | A10 | 19114875 | C | T | upstream_gene_variant | MODIFIER | c.-7C>T| |
S168 |
| 4 | BAA10g21950 | A10 | 19115314 | G | A | missense_variant | MODERATE | c.433G>A|p.Val145Met |
S36 |
| 5 | BAA10g21950 | A10 | 19115487 | C | T | missense_variant | MODERATE | c.532C>T|p.Leu178Phe |
S255 |
| 6 | BAA10g21950 | A10 | 19115632 | C | T | missense_variant | MODERATE | c.677C>T|p.Ala226Val |
S122 |
| 7 | BAA10g21950 | A10 | 19116603 | C | T | stop_gained | HIGH | c.1648C>T|p.Gln550* |
S48 |
| 8 | BAA10g21950 | A10 | 19117365 | C | T | missense_variant | MODERATE | c.2240C>T|p.Ser747Phe |
S10 |
| 9 | BAA10g21950 | A10 | 19117377 | G | A | missense_variant | MODERATE | c.2252G>A|p.Ser751Asn |
S295 |
| 10 | BAA10g21950 | A10 | 19117920 | G | A | missense_variant | MODERATE | c.2795G>A|p.Arg932Lys |
S294 |
| 11 | BAA10g21950 | A10 | 19117999 | C | T | synonymous_variant | LOW | c.2874C>T|p.Leu958Leu |
S133 |
| 12 | BAA10g21950 | A10 | 19118539 | C | T | synonymous_variant | LOW | c.3414C>T|p.Ala1138Ala |
S283 |
| 13 | BAA10g21950 | A10 | 19118997 | G | A | missense_variant | MODERATE | c.3872G>A|p.Cys1291Tyr |
S1 S90 |
| 14 | BAA10g21950 | A10 | 19119176 | G | A | missense_variant | MODERATE | c.4051G>A|p.Val1351Ile |
S178 |