Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19990 | A10 | 18159854 | C | T | upstream_gene_variant | MODIFIER | c.-3709C>T| |
S26 |
2 | BAA10g19990 | A10 | 18160138 | G | A | upstream_gene_variant | MODIFIER | c.-3425G>A| |
S1 S90 |
3 | BAA10g19990 | A10 | 18160756 | C | T | upstream_gene_variant | MODIFIER | c.-2807C>T| |
S199 |
4 | BAA10g19990 | A10 | 18160757 | G | A | upstream_gene_variant | MODIFIER | c.-2806G>A| |
S63 |
5 | BAA10g19990 | A10 | 18161511 | G | A | upstream_gene_variant | MODIFIER | c.-2052G>A| |
S283 |
6 | BAA10g19990 | A10 | 18161960 | C | T | upstream_gene_variant | MODIFIER | c.-1603C>T| |
S286 |
7 | BAA10g19990 | A10 | 18163214 | G | A | upstream_gene_variant | MODIFIER | c.-349G>A| |
S131 |
8 | BAA10g19990 | A10 | 18163702 | G | A | missense_variant | MODERATE | c.140G>A|p.Cys47Tyr |
S231 |
9 | BAA10g19990 | A10 | 18163759 | C | T | missense_variant | MODERATE | c.197C>T|p.Ala66Val |
S152 |
10 | BAA10g19990 | A10 | 18163919 | C | T | synonymous_variant | LOW | c.357C>T|p.Gly119Gly |
S210 S225 |
11 | BAA10g19990 | A10 | 18163944 | G | A | missense_variant | MODERATE | c.382G>A|p.Gly128Ser |
S66 |