Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19690 | A10 | 17987190 | G | A | downstream_gene_variant | MODIFIER | c.*2934C>T| |
S208 S219 |
2 | BAA10g19690 | A10 | 17987364 | G | A | downstream_gene_variant | MODIFIER | c.*2760C>T| |
S212 |
3 | BAA10g19690 | A10 | 17987662 | G | A | downstream_gene_variant | MODIFIER | c.*2462C>T| |
S165 |
4 | BAA10g19690 | A10 | 17988717 | C | T | downstream_gene_variant | MODIFIER | c.*1407G>A| |
S281 |
5 | BAA10g19690 | A10 | 17990155 | C | T | missense_variant | MODERATE | c.2120G>A|p.Ser707Asn |
S119 |
6 | BAA10g19690 | A10 | 17990774 | C | T | missense_variant | MODERATE | c.1756G>A|p.Val586Met |
S51 |
7 | BAA10g19690 | A10 | 17990857 | C | T | missense_variant | MODERATE | c.1673G>A|p.Gly558Glu |
S170 |
8 | BAA10g19690 | A10 | 17991640 | G | A | missense_variant | MODERATE | c.1580C>T|p.Ser527Leu |
S184 |
9 | BAA10g19690 | A10 | 17991778 | C | T | missense_variant | MODERATE | c.1442G>A|p.Arg481His |
S259 |
10 | BAA10g19690 | A10 | 17991800 | C | T | missense_variant | MODERATE | c.1420G>A|p.Asp474Asn |
S46 |
11 | BAA10g19690 | A10 | 17992172 | C | T | missense_variant | MODERATE | c.1048G>A|p.Asp350Asn |
S116 |
12 | BAA10g19690 | A10 | 17992228 | G | A | missense_variant | MODERATE | c.992C>T|p.Ser331Phe |
S39 |
13 | BAA10g19690 | A10 | 17992388 | C | T | missense_variant | MODERATE | c.832G>A|p.Glu278Lys |
S283 |
14 | BAA10g19690 | A10 | 17993468 | G | A | missense_variant | MODERATE | c.490C>T|p.Pro164Ser |
S279 |
15 | BAA10g19690 | A10 | 17995056 | C | T | upstream_gene_variant | MODIFIER | c.-927G>A| |
S189 |
16 | BAA10g19690 | A10 | 17995118 | C | T | upstream_gene_variant | MODIFIER | c.-989G>A| |
S156 |
17 | BAA10g19690 | A10 | 17995565 | C | T | upstream_gene_variant | MODIFIER | c.-1436G>A| |
S199 |
18 | BAA10g19690 | A10 | 17995989 | C | T | upstream_gene_variant | MODIFIER | c.-1860G>A| |
S99 |
19 | BAA10g19690 | A10 | 17997507 | C | T | upstream_gene_variant | MODIFIER | c.-3378G>A| |
S251 |