Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g33990 | A02 | 29106637 | G | A | synonymous_variant | LOW | c.1584C>T|p.Gly528Gly |
S210 |
2 | BAA02g33990 | A02 | 29106716 | C | T | missense_variant | MODERATE | c.1505G>A|p.Arg502Lys |
S46 |
3 | BAA02g33990 | A02 | 29106979 | G | A | synonymous_variant | LOW | c.1242C>T|p.Leu414Leu |
S217 S248 |
4 | BAA02g33990 | A02 | 29107107 | C | T | missense_variant | MODERATE | c.1114G>A|p.Glu372Lys |
S78 S83 |
5 | BAA02g33990 | A02 | 29108798 | G | A | synonymous_variant | LOW | c.135C>T|p.Pro45Pro |
S251 |
6 | BAA02g33990 | A02 | 29108865 | G | A | missense_variant | MODERATE | c.68C>T|p.Ser23Phe |
S148 |
7 | BAA02g33990 | A02 | 29109188 | G | A | upstream_gene_variant | MODIFIER | c.-256C>T| |
S148 |
8 | BAA02g33990 | A02 | 29109366 | C | T | upstream_gene_variant | MODIFIER | c.-434G>A| |
S165 |
9 | BAA02g33990 | A02 | 29110457 | C | T | upstream_gene_variant | MODIFIER | c.-1525G>A| |
S273 |
10 | BAA02g33990 | A02 | 29111839 | G | A | upstream_gene_variant | MODIFIER | c.-2907C>T| |
S10 |
11 | BAA02g33990 | A02 | 29112048 | T | A | upstream_gene_variant | MODIFIER | c.-3116A>T| |
S94 |
12 | BAA02g33990 | A02 | 29112321 | G | A | upstream_gene_variant | MODIFIER | c.-3389C>T| |
S85 |
13 | BAA02g33990 | A02 | 29112556 | G | A | upstream_gene_variant | MODIFIER | c.-3624C>T| |
S266 |
14 | BAA02g33990 | A02 | 29112806 | C | T | upstream_gene_variant | MODIFIER | c.-3874G>A| |
S284 |