Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13140 | A08 | 11396858 | G | A | upstream_gene_variant | MODIFIER | c.-4577G>A| |
S33 |
2 | BAA08g13140 | A08 | 11396892 | C | T | upstream_gene_variant | MODIFIER | c.-4543C>T| |
S114 |
3 | BAA08g13140 | A08 | 11397488 | A | T | upstream_gene_variant | MODIFIER | c.-3947A>T| |
S92 |
4 | BAA08g13140 | A08 | 11397520 | C | T | upstream_gene_variant | MODIFIER | c.-3915C>T| |
S205 |
5 | BAA08g13140 | A08 | 11398170 | C | T | upstream_gene_variant | MODIFIER | c.-3265C>T| |
S135 |
6 | BAA08g13140 | A08 | 11398952 | G | A | upstream_gene_variant | MODIFIER | c.-2483G>A| |
S218 |
7 | BAA08g13140 | A08 | 11399399 | G | A | upstream_gene_variant | MODIFIER | c.-2036G>A| |
S117 |
8 | BAA08g13140 | A08 | 11400181 | G | A | upstream_gene_variant | MODIFIER | c.-1254G>A| |
S266 |
9 | BAA08g13140 | A08 | 11401438 | G | A | missense_variant | MODERATE | c.4G>A|p.Val2Met |
S158 |
10 | BAA08g13140 | A08 | 11401795 | G | A | missense_variant | MODERATE | c.361G>A|p.Glu121Lys |
S188 |
11 | BAA08g13140 | A08 | 11402701 | G | A | intron_variant | MODIFIER | c.1192-11G>A| |
S58 |
12 | BAA08g13140 | A08 | 11404973 | C | T | intron_variant | MODIFIER | c.1617+1753C>T| |
S215 |
13 | BAA08g13140 | A08 | 11405528 | C | T | intron_variant | MODIFIER | c.1617+2308C>T| |
S8 |
14 | BAA08g13140 | A08 | 11405602 | G | A | intron_variant | MODIFIER | c.1617+2382G>A| |
S260 |
15 | BAA08g13140 | A08 | 11410612 | C | T | downstream_gene_variant | MODIFIER | c.*88C>T| |
S197 |
16 | BAA08g13140 | A08 | 11410778 | T | G | downstream_gene_variant | MODIFIER | c.*254T>G| |
S226 S255 S280 S299 |