Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g30770 | A01 | 19712787 | C | T | downstream_gene_variant | MODIFIER | c.*723G>A| |
S136 |
2 | BAA01g30770 | A01 | 19712809 | C | T | downstream_gene_variant | MODIFIER | c.*701G>A| |
S240 |
3 | BAA01g30770 | A01 | 19712924 | C | T | downstream_gene_variant | MODIFIER | c.*586G>A| |
S57 |
4 | BAA01g30770 | A01 | 19713041 | C | T | downstream_gene_variant | MODIFIER | c.*469G>A| |
S206 S26 |
5 | BAA01g30770 | A01 | 19713865 | C | T | intron_variant | MODIFIER | c.577-155G>A| |
S284 |
6 | BAA01g30770 | A01 | 19713966 | G | A | intron_variant | MODIFIER | c.577-256C>T| |
S149 |
7 | BAA01g30770 | A01 | 19714491 | G | A | intron_variant | MODIFIER | c.576+66C>T| |
S116 |
8 | BAA01g30770 | A01 | 19715011 | C | T | synonymous_variant | LOW | c.447G>A|p.Lys149Lys |
S303 |
9 | BAA01g30770 | A01 | 19715041 | C | T | synonymous_variant | LOW | c.417G>A|p.Arg139Arg |
S81 S85 |
10 | BAA01g30770 | A01 | 19715088 | C | T | missense_variant | MODERATE | c.370G>A|p.Glu124Lys |
S39 |
11 | BAA01g30770 | A01 | 19715338 | C | T | synonymous_variant | LOW | c.120G>A|p.Lys40Lys |
S76 |
12 | BAA01g30770 | A01 | 19716390 | C | T | upstream_gene_variant | MODIFIER | c.-933G>A| |
S75 S81 |
13 | BAA01g30770 | A01 | 19716611 | G | A | upstream_gene_variant | MODIFIER | c.-1154C>T| |
S207 |
14 | BAA01g30770 | A01 | 19716959 | C | T | upstream_gene_variant | MODIFIER | c.-1502G>A| |
S171 |
15 | BAA01g30770 | A01 | 19717650 | G | A | upstream_gene_variant | MODIFIER | c.-2193C>T| |
S280 |
16 | BAA01g30770 | A01 | 19717766 | G | A | upstream_gene_variant | MODIFIER | c.-2309C>T| |
S86 |
17 | BAA01g30770 | A01 | 19718261 | C | T | upstream_gene_variant | MODIFIER | c.-2804G>A| |
S282 |
18 | BAA01g30770 | A01 | 19719927 | C | G | upstream_gene_variant | MODIFIER | c.-4470G>C| |
S116 |