Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g21250 | A05 | 13487475 | C | T | downstream_gene_variant | MODIFIER | c.*2618G>A| |
S12 |
2 | BAA05g21250 | A05 | 13491680 | C | T | synonymous_variant | LOW | c.1482G>A|p.Gln494Gln |
S17 |
3 | BAA05g21250 | A05 | 13491763 | C | T | missense_variant | MODERATE | c.1399G>A|p.Glu467Lys |
S100 |
4 | BAA05g21250 | A05 | 13491859 | C | T | missense_variant | MODERATE | c.1303G>A|p.Glu435Lys |
S193 |
5 | BAA05g21250 | A05 | 13491911 | C | T | synonymous_variant | LOW | c.1251G>A|p.Thr417Thr |
S68 |
6 | BAA05g21250 | A05 | 13491987 | C | T | missense_variant | MODERATE | c.1175G>A|p.Gly392Glu |
S208 S93 |
7 | BAA05g21250 | A05 | 13492231 | C | T | missense_variant | MODERATE | c.931G>A|p.Gly311Arg |
S28 |
8 | BAA05g21250 | A05 | 13493042 | G | A | synonymous_variant | LOW | c.120C>T|p.Leu40Leu |
S125 |
9 | BAA05g21250 | A05 | 13493113 | G | A | missense_variant | MODERATE | c.49C>T|p.Arg17Cys |
S151 S263 |
10 | BAA05g21250 | A05 | 13497575 | C | T | upstream_gene_variant | MODIFIER | c.-4414G>A| |
S135 |
11 | BAA05g21250 | A05 | 13497580 | G | A | upstream_gene_variant | MODIFIER | c.-4419C>T| |
S178 |
12 | BAA05g21250 | A05 | 13497584 | G | A | upstream_gene_variant | MODIFIER | c.-4423C>T| |
S288 |
13 | BAA05g21250 | A05 | 13498034 | C | T | upstream_gene_variant | MODIFIER | c.-4873G>A| |
S57 |