Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g02000 | A03 | 905445 | G | A | downstream_gene_variant | MODIFIER | c.*1758C>T| |
S162 |
2 | BAA03g02000 | A03 | 905606 | G | A | downstream_gene_variant | MODIFIER | c.*1597C>T| |
S206 S26 |
3 | BAA03g02000 | A03 | 907429 | C | T | missense_variant | MODERATE | c.1568G>A|p.Gly523Glu |
S122 |
4 | BAA03g02000 | A03 | 907464 | G | A | synonymous_variant | LOW | c.1533C>T|p.Ile511Ile |
S17 |
5 | BAA03g02000 | A03 | 907649 | G | A | missense_variant | MODERATE | c.1348C>T|p.Arg450Cys |
S36 |
6 | BAA03g02000 | A03 | 908307 | C | T | missense_variant | MODERATE | c.886G>A|p.Glu296Lys |
S263 |
7 | BAA03g02000 | A03 | 909895 | C | T | synonymous_variant | LOW | c.603G>A|p.Thr201Thr |
S53 |
8 | BAA03g02000 | A03 | 910149 | C | T | missense_variant | MODERATE | c.349G>A|p.Asp117Asn |
S82 S92 |
9 | BAA03g02000 | A03 | 911109 | C | T | upstream_gene_variant | MODIFIER | c.-612G>A| |
S268 |
10 | BAA03g02000 | A03 | 911779 | G | A | upstream_gene_variant | MODIFIER | c.-1282C>T| |
S69 |
11 | BAA03g02000 | A03 | 912434 | G | A | upstream_gene_variant | MODIFIER | c.-1937C>T| |
S116 |
12 | BAA03g02000 | A03 | 913239 | C | T | upstream_gene_variant | MODIFIER | c.-2742G>A| |
S308 |
13 | BAA03g02000 | A03 | 915315 | G | A | upstream_gene_variant | MODIFIER | c.-4818C>T| |
S183 S198 |