Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22770 | A02 | 12338090 | C | T | downstream_gene_variant | MODIFIER | c.*2132G>A| |
S11 |
2 | BAA02g22770 | A02 | 12340497 | C | T | missense_variant | MODERATE | c.190G>A|p.Glu64Lys |
S159 S188 S243 S276 S298 S299 |
3 | BAA02g22770 | A02 | 12340605 | C | T | missense_variant | MODERATE | c.82G>A|p.Glu28Lys |
S266 |
4 | BAA02g22770 | A02 | 12341435 | C | T | upstream_gene_variant | MODIFIER | c.-749G>A| |
S52 |
5 | BAA02g22770 | A02 | 12341859 | G | A | upstream_gene_variant | MODIFIER | c.-1173C>T| |
S125 |
6 | BAA02g22770 | A02 | 12341893 | C | T | upstream_gene_variant | MODIFIER | c.-1207G>A| |
S283 |
7 | BAA02g22770 | A02 | 12342824 | C | T | upstream_gene_variant | MODIFIER | c.-2138G>A| |
S40 S49 |
8 | BAA02g22770 | A02 | 12343011 | C | T | upstream_gene_variant | MODIFIER | c.-2325G>A| |
S80 |
9 | BAA02g22770 | A02 | 12343716 | C | T | upstream_gene_variant | MODIFIER | c.-3030G>A| |
S299 S71 |
10 | BAA02g22770 | A02 | 12345423 | G | A | upstream_gene_variant | MODIFIER | c.-4737C>T| |
S35 |