Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g42990 | A01 | 28457168 | C | T | upstream_gene_variant | MODIFIER | c.-4961C>T| |
S134 |
2 | BAA01g42990 | A01 | 28458559 | G | A | upstream_gene_variant | MODIFIER | c.-3570G>A| |
S85 |
3 | BAA01g42990 | A01 | 28459017 | C | T | upstream_gene_variant | MODIFIER | c.-3112C>T| |
S77 |
4 | BAA01g42990 | A01 | 28459885 | T | A | upstream_gene_variant | MODIFIER | c.-2244T>A| |
S166 |
5 | BAA01g42990 | A01 | 28459969 | G | A | upstream_gene_variant | MODIFIER | c.-2160G>A| |
S208 S219 |
6 | BAA01g42990 | A01 | 28460866 | C | T | upstream_gene_variant | MODIFIER | c.-1263C>T| |
S260 |
7 | BAA01g42990 | A01 | 28460899 | C | T | upstream_gene_variant | MODIFIER | c.-1230C>T| |
S62 |
8 | BAA01g42990 | A01 | 28461433 | C | T | upstream_gene_variant | MODIFIER | c.-696C>T| |
S44 |
9 | BAA01g42990 | A01 | 28464520 | G | A | splice_donor_variant&intron_variant | HIGH | c.1155+1G>A| |
S1 S90 |
10 | BAA01g42990 | A01 | 28464652 | C | T | missense_variant | MODERATE | c.1201C>T|p.Leu401Phe |
S51 S52 |
11 | BAA01g42990 | A01 | 28464874 | G | A | missense_variant | MODERATE | c.1279G>A|p.Ala427Thr |
S108 |
12 | BAA01g42990 | A01 | 28465455 | G | A | downstream_gene_variant | MODIFIER | c.*207G>A| |
S268 |