Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26630 | A10 | 21055224 | G | A | upstream_gene_variant | MODIFIER | c.-692G>A| |
S263 |
2 | BAA10g26630 | A10 | 21055349 | C | T | upstream_gene_variant | MODIFIER | c.-567C>T| |
S168 |
3 | BAA10g26630 | A10 | 21055428 | G | A | upstream_gene_variant | MODIFIER | c.-488G>A| |
S256 |
4 | BAA10g26630 | A10 | 21055575 | C | T | upstream_gene_variant | MODIFIER | c.-341C>T| |
S68 |
5 | BAA10g26630 | A10 | 21055935 | C | T | missense_variant | MODERATE | c.20C>T|p.Ala7Val |
S25 |
6 | BAA10g26630 | A10 | 21056526 | G | A | stop_gained | HIGH | c.611G>A|p.Trp204* |
S112 |
7 | BAA10g26630 | A10 | 21056624 | C | T | stop_gained | HIGH | c.709C>T|p.Gln237* |
S5 |
8 | BAA10g26630 | A10 | 21057130 | C | T | missense_variant | MODERATE | c.881C>T|p.Ala294Val |
S168 |
9 | BAA10g26630 | A10 | 21057138 | G | A | missense_variant | MODERATE | c.889G>A|p.Ala297Thr |
S50 |