Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g33700 | A01 | 22463233 | C | T | upstream_gene_variant | MODIFIER | c.-1508C>T| |
S79 S84 |
2 | BAA01g33700 | A01 | 22463345 | G | A | upstream_gene_variant | MODIFIER | c.-1396G>A| |
S15 |
3 | BAA01g33700 | A01 | 22463482 | A | C | upstream_gene_variant | MODIFIER | c.-1259A>C| |
S166 |
4 | BAA01g33700 | A01 | 22463640 | C | T | upstream_gene_variant | MODIFIER | c.-1101C>T| |
S255 |
5 | BAA01g33700 | A01 | 22463673 | G | A | upstream_gene_variant | MODIFIER | c.-1068G>A| |
S38 |
6 | BAA01g33700 | A01 | 22463760 | C | T | upstream_gene_variant | MODIFIER | c.-981C>T| |
S183 S198 S219 S72 |
7 | BAA01g33700 | A01 | 22463848 | G | A | upstream_gene_variant | MODIFIER | c.-893G>A| |
S308 |
8 | BAA01g33700 | A01 | 22464581 | C | T | upstream_gene_variant | MODIFIER | c.-160C>T| |
S233 |
9 | BAA01g33700 | A01 | 22466311 | C | T | missense_variant | MODERATE | c.1571C>T|p.Ala524Val |
S67 |
10 | BAA01g33700 | A01 | 22467246 | G | A | missense_variant | MODERATE | c.2270G>A|p.Arg757His |
S176 |
11 | BAA01g33700 | A01 | 22467414 | C | T | missense_variant | MODERATE | c.2333C>T|p.Pro778Leu |
S53 |
12 | BAA01g33700 | A01 | 22467561 | C | T | missense_variant | MODERATE | c.2401C>T|p.Pro801Ser |
S53 |
13 | BAA01g33700 | A01 | 22467748 | C | T | downstream_gene_variant | MODIFIER | c.*2C>T| |
S177 |
14 | BAA01g33700 | A01 | 22470091 | G | A | downstream_gene_variant | MODIFIER | c.*2345G>A| |
S202 |
15 | BAA01g33700 | A01 | 22470257 | C | T | downstream_gene_variant | MODIFIER | c.*2511C>T| |
S81 |
16 | BAA01g33700 | A01 | 22470389 | G | A | downstream_gene_variant | MODIFIER | c.*2643G>A| |
S262 |