Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g15080 | A04 | 19961209 | G | A | downstream_gene_variant | MODIFIER | c.*1742C>T| |
S114 |
2 | BAA04g15080 | A04 | 19961422 | G | A | downstream_gene_variant | MODIFIER | c.*1529C>T| |
S53 |
3 | BAA04g15080 | A04 | 19961651 | C | T | downstream_gene_variant | MODIFIER | c.*1300G>A| |
S293 |
4 | BAA04g15080 | A04 | 19961734 | C | T | downstream_gene_variant | MODIFIER | c.*1217G>A| |
S295 |
5 | BAA04g15080 | A04 | 19963076 | C | G | intron_variant | MODIFIER | c.1311-38G>C| |
S211 S227 |
6 | BAA04g15080 | A04 | 19963224 | C | T | synonymous_variant | LOW | c.1233G>A|p.Gly411Gly |
S64 |
7 | BAA04g15080 | A04 | 19963600 | G | A | intron_variant | MODIFIER | c.1185+167C>T| |
S156 |
8 | BAA04g15080 | A04 | 19965633 | C | T | intron_variant | MODIFIER | c.517-366G>A| |
S98 |
9 | BAA04g15080 | A04 | 19965850 | G | A | intron_variant | MODIFIER | c.517-583C>T| |
S47 |
10 | BAA04g15080 | A04 | 19965864 | G | T | intron_variant | MODIFIER | c.516+589C>A| |
S153 |
11 | BAA04g15080 | A04 | 19966087 | G | A | intron_variant | MODIFIER | c.516+366C>T| |
S286 |
12 | BAA04g15080 | A04 | 19966221 | C | T | intron_variant | MODIFIER | c.516+232G>A| |
S281 |
13 | BAA04g15080 | A04 | 19966803 | G | A | intron_variant | MODIFIER | c.192-26C>T| |
S123 |
14 | BAA04g15080 | A04 | 19966976 | G | A | synonymous_variant | LOW | c.66C>T|p.Leu22Leu |
S182 |
15 | BAA04g15080 | A04 | 19969164 | G | A | upstream_gene_variant | MODIFIER | c.-2123C>T| |
S59 |
16 | BAA04g15080 | A04 | 19969670 | C | T | upstream_gene_variant | MODIFIER | c.-2629G>A| |
S247 |
17 | BAA04g15080 | A04 | 19969980 | G | A | upstream_gene_variant | MODIFIER | c.-2939C>T| |
S191 |
18 | BAA04g15080 | A04 | 19970657 | C | T | upstream_gene_variant | MODIFIER | c.-3616G>A| |
S64 |
19 | BAA04g15080 | A04 | 19970946 | G | A | upstream_gene_variant | MODIFIER | c.-3905C>T| |
S191 |
20 | BAA04g15080 | A04 | 19971678 | G | A | upstream_gene_variant | MODIFIER | c.-4637C>T| |
S208 |