Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g62660 | A03 | 31823103 | C | T | upstream_gene_variant | MODIFIER | c.-4472C>T| |
S34 |
2 | BAA03g62660 | A03 | 31823887 | G | A | upstream_gene_variant | MODIFIER | c.-3688G>A| |
S25 |
3 | BAA03g62660 | A03 | 31828982 | C | T | missense_variant | MODERATE | c.1261C>T|p.Leu421Phe |
S40 S49 |
4 | BAA03g62660 | A03 | 31829243 | C | T | synonymous_variant | LOW | c.1522C>T|p.Leu508Leu |
S189 |
5 | BAA03g62660 | A03 | 31829297 | A | T | missense_variant | MODERATE | c.1576A>T|p.Met526Leu |
S45 |
6 | BAA03g62660 | A03 | 31829320 | G | A | synonymous_variant | LOW | c.1599G>A|p.Leu533Leu |
S1 S90 |
7 | BAA03g62660 | A03 | 31829378 | G | A | missense_variant | MODERATE | c.1657G>A|p.Glu553Lys |
S133 |
8 | BAA03g62660 | A03 | 31829435 | G | A | intron_variant | MODIFIER | c.1686+28G>A| |
S223 |
9 | BAA03g62660 | A03 | 31833333 | G | A | synonymous_variant | LOW | c.2070G>A|p.Glu690Glu |
S247 |
10 | BAA03g62660 | A03 | 31833337 | G | A | missense_variant | MODERATE | c.2074G>A|p.Val692Ile |
S122 |
11 | BAA03g62660 | A03 | 31835875 | C | T | downstream_gene_variant | MODIFIER | c.*2314C>T| |
S15 S3 |