Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28740 | A10 | 21911951 | G | A | upstream_gene_variant | MODIFIER | c.-4816G>A| |
S108 |
2 | BAA10g28740 | A10 | 21912564 | G | A | upstream_gene_variant | MODIFIER | c.-4203G>A| |
S293 |
3 | BAA10g28740 | A10 | 21912839 | C | T | upstream_gene_variant | MODIFIER | c.-3928C>T| |
S129 |
4 | BAA10g28740 | A10 | 21912857 | C | T | upstream_gene_variant | MODIFIER | c.-3910C>T| |
S13 |
5 | BAA10g28740 | A10 | 21913226 | C | T | upstream_gene_variant | MODIFIER | c.-3541C>T| |
S166 |
6 | BAA10g28740 | A10 | 21917046 | G | A | missense_variant | MODERATE | c.205G>A|p.Val69Ile |
S219 S72 |
7 | BAA10g28740 | A10 | 21917257 | C | T | missense_variant | MODERATE | c.416C>T|p.Ser139Phe |
S305 |
8 | BAA10g28740 | A10 | 21917269 | G | A | missense_variant | MODERATE | c.428G>A|p.Arg143Lys |
S42 |
9 | BAA10g28740 | A10 | 21917897 | C | T | synonymous_variant | LOW | c.1056C>T|p.Thr352Thr |
S189 |