Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g09130 | A07 | 18062285 | G | A | missense_variant | MODERATE | c.1073C>T|p.Thr358Ile |
S155 S211 |
2 | BAA07g09130 | A07 | 18062617 | C | T | missense_variant | MODERATE | c.1025G>A|p.Arg342His |
S155 S211 |
3 | BAA07g09130 | A07 | 18062766 | G | A | missense_variant | MODERATE | c.950C>T|p.Ser317Leu |
S233 |
4 | BAA07g09130 | A07 | 18062949 | C | T | missense_variant | MODERATE | c.856G>A|p.Glu286Lys |
S47 |
5 | BAA07g09130 | A07 | 18065694 | G | A | upstream_gene_variant | MODIFIER | c.-110C>T| |
S308 |
6 | BAA07g09130 | A07 | 18066575 | G | A | upstream_gene_variant | MODIFIER | c.-991C>T| |
S202 |
7 | BAA07g09130 | A07 | 18066661 | G | A | upstream_gene_variant | MODIFIER | c.-1077C>T| |
S157 S163 |
8 | BAA07g09130 | A07 | 18067227 | C | T | upstream_gene_variant | MODIFIER | c.-1643G>A| |
S34 |
9 | BAA07g09130 | A07 | 18067298 | C | T | upstream_gene_variant | MODIFIER | c.-1714G>A| |
S70 |
10 | BAA07g09130 | A07 | 18067536 | C | T | upstream_gene_variant | MODIFIER | c.-1952G>A| |
S267 |
11 | BAA07g09130 | A07 | 18068124 | G | A | upstream_gene_variant | MODIFIER | c.-2540C>T| |
S61 |
12 | BAA07g09130 | A07 | 18068270 | G | A | upstream_gene_variant | MODIFIER | c.-2686C>T| |
S288 |
13 | BAA07g09130 | A07 | 18068305 | C | T | upstream_gene_variant | MODIFIER | c.-2721G>A| |
S189 |
14 | BAA07g09130 | A07 | 18068962 | C | T | upstream_gene_variant | MODIFIER | c.-3378G>A| |
S231 |
15 | BAA07g09130 | A07 | 18070372 | C | T | upstream_gene_variant | MODIFIER | c.-4788G>A| |
S192 |