Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04580 | A10 | 2332936 | C | T | missense_variant | MODERATE | c.2134G>A|p.Val712Ile |
S130 |
2 | BAA10g04580 | A10 | 2333546 | C | T | synonymous_variant | LOW | c.1524G>A|p.Gly508Gly |
S181 |
3 | BAA10g04580 | A10 | 2334619 | G | A | stop_gained | HIGH | c.451C>T|p.Gln151* |
S236 |
4 | BAA10g04580 | A10 | 2334685 | C | T | missense_variant | MODERATE | c.385G>A|p.Val129Met |
S162 |
5 | BAA10g04580 | A10 | 2334963 | G | A | missense_variant | MODERATE | c.107C>T|p.Pro36Leu |
S67 |
6 | BAA10g04580 | A10 | 2336910 | C | T | upstream_gene_variant | MODIFIER | c.-1841G>A| |
S122 |
7 | BAA10g04580 | A10 | 2339658 | C | T | upstream_gene_variant | MODIFIER | c.-4589G>A| |
S115 |
8 | BAA10g04580 | A10 | 2339710 | G | A | upstream_gene_variant | MODIFIER | c.-4641C>T| |
S112 |
9 | BAA10g04580 | A10 | 2340020 | G | A | upstream_gene_variant | MODIFIER | c.-4951C>T| |
S17 |