Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00230 | A10 | 105519 | C | T | missense_variant | MODERATE | c.3085G>A|p.Gly1029Arg |
S56 |
2 | BAA10g00230 | A10 | 105526 | G | A | synonymous_variant | LOW | c.3078C>T|p.Asp1026Asp |
S262 |
3 | BAA10g00230 | A10 | 106816 | G | A | synonymous_variant | LOW | c.2464C>T|p.Leu822Leu |
S50 |
4 | BAA10g00230 | A10 | 107087 | G | A | stop_gained | HIGH | c.2287C>T|p.Arg763* |
S39 |
5 | BAA10g00230 | A10 | 109425 | G | A | missense_variant | MODERATE | c.886C>T|p.Arg296Cys |
S83 S88 |
6 | BAA10g00230 | A10 | 109659 | C | T | missense_variant | MODERATE | c.652G>A|p.Glu218Lys |
S67 |
7 | BAA10g00230 | A10 | 110061 | C | T | missense_variant | MODERATE | c.250G>A|p.Glu84Lys |
S283 |
8 | BAA10g00230 | A10 | 110388 | G | A | upstream_gene_variant | MODIFIER | c.-78C>T| |
S38 |
9 | BAA10g00230 | A10 | 110448 | G | A | upstream_gene_variant | MODIFIER | c.-138C>T| |
S166 |
10 | BAA10g00230 | A10 | 114032 | C | T | upstream_gene_variant | MODIFIER | c.-3722G>A| |
S143 |
11 | BAA10g00230 | A10 | 114118 | C | T | upstream_gene_variant | MODIFIER | c.-3808G>A| |
S130 |
12 | BAA10g00230 | A10 | 114204 | C | T | upstream_gene_variant | MODIFIER | c.-3894G>A| |
S204 |
13 | BAA10g00230 | A10 | 114531 | C | T | upstream_gene_variant | MODIFIER | c.-4221G>A| |
S238 |