Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28600 | A02 | 16080738 | G | A | downstream_gene_variant | MODIFIER | c.*2529C>T| |
S5 |
2 | BAA02g28600 | A02 | 16080962 | G | A | downstream_gene_variant | MODIFIER | c.*2305C>T| |
S136 |
3 | BAA02g28600 | A02 | 16081587 | G | A | downstream_gene_variant | MODIFIER | c.*1680C>T| |
S92 |
4 | BAA02g28600 | A02 | 16081620 | C | T | downstream_gene_variant | MODIFIER | c.*1647G>A| |
S303 |
5 | BAA02g28600 | A02 | 16083364 | G | A | missense_variant | MODERATE | c.878C>T|p.Thr293Ile |
S157 |
6 | BAA02g28600 | A02 | 16084021 | G | A | missense_variant | MODERATE | c.455C>T|p.Ser152Leu |
S68 |
7 | BAA02g28600 | A02 | 16084245 | G | A | missense_variant | MODERATE | c.329C>T|p.Ser110Phe |
S173 |
8 | BAA02g28600 | A02 | 16084287 | G | A | missense_variant | MODERATE | c.287C>T|p.Ala96Val |
S278 |
9 | BAA02g28600 | A02 | 16084419 | C | T | intron_variant | MODIFIER | c.219+45G>A| |
S87 |
10 | BAA02g28600 | A02 | 16084839 | G | A | upstream_gene_variant | MODIFIER | c.-157C>T| |
S105 S106 |
11 | BAA02g28600 | A02 | 16084841 | G | A | upstream_gene_variant | MODIFIER | c.-159C>T| |
S256 |
12 | BAA02g28600 | A02 | 16085394 | G | A | upstream_gene_variant | MODIFIER | c.-712C>T| |
S25 |
13 | BAA02g28600 | A02 | 16086228 | C | T | upstream_gene_variant | MODIFIER | c.-1546G>A| |
S40 |
14 | BAA02g28600 | A02 | 16086407 | G | A | upstream_gene_variant | MODIFIER | c.-1725C>T| |
S122 |
15 | BAA02g28600 | A02 | 16086449 | C | T | upstream_gene_variant | MODIFIER | c.-1767G>A| |
S276 |
16 | BAA02g28600 | A02 | 16086640 | G | T | upstream_gene_variant | MODIFIER | c.-1958C>A| |
S162 |
17 | BAA02g28600 | A02 | 16087075 | G | A | upstream_gene_variant | MODIFIER | c.-2393C>T| |
S150 |
18 | BAA02g28600 | A02 | 16087880 | C | T | upstream_gene_variant | MODIFIER | c.-3198G>A| |
S183 S198 |
19 | BAA02g28600 | A02 | 16089369 | C | T | upstream_gene_variant | MODIFIER | c.-4687G>A| |
S2 |
20 | BAA02g28600 | A02 | 16089577 | G | A | upstream_gene_variant | MODIFIER | c.-4895C>T| |
S17 |
21 | BAA02g28600 | A02 | 16089582 | C | T | upstream_gene_variant | MODIFIER | c.-4900G>A| |
S18 |