Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g45700 | A03 | 21912412 | G | A | downstream_gene_variant | MODIFIER | c.*1948C>T| |
S233 |
2 | BAA03g45700 | A03 | 21914571 | T | G | missense_variant | MODERATE | c.3620A>C|p.Gln1207Pro |
S142 S200 S206 S261 S274 S28 S292 S61 |
3 | BAA03g45700 | A03 | 21914872 | C | T | missense_variant | MODERATE | c.3401G>A|p.Gly1134Glu |
S176 |
4 | BAA03g45700 | A03 | 21915179 | C | T | missense_variant | MODERATE | c.3094G>A|p.Val1032Met |
S117 |
5 | BAA03g45700 | A03 | 21915891 | G | A | synonymous_variant | LOW | c.2568C>T|p.Leu856Leu |
S64 |
6 | BAA03g45700 | A03 | 21916271 | G | A | synonymous_variant | LOW | c.2358C>T|p.Val786Val |
S260 |
7 | BAA03g45700 | A03 | 21916694 | C | T | splice_donor_variant&intron_variant | HIGH | c.2196+1G>A| |
S113 |
8 | BAA03g45700 | A03 | 21918214 | C | T | missense_variant | MODERATE | c.1370G>A|p.Gly457Asp |
S11 |
9 | BAA03g45700 | A03 | 21919541 | C | T | missense_variant&splice_region_variant | MODERATE | c.665G>A|p.Ser222Asn |
S190 |
10 | BAA03g45700 | A03 | 21919661 | C | T | missense_variant | MODERATE | c.545G>A|p.Gly182Asp |
S66 |
11 | BAA03g45700 | A03 | 21919925 | G | A | missense_variant | MODERATE | c.380C>T|p.Thr127Ile |
S167 |
12 | BAA03g45700 | A03 | 21920252 | G | A | missense_variant | MODERATE | c.125C>T|p.Ser42Leu |
S71 |
13 | BAA03g45700 | A03 | 21920478 | C | T | synonymous_variant | LOW | c.6G>A|p.Glu2Glu |
S42 |
14 | BAA03g45700 | A03 | 21920492 | C | T | upstream_gene_variant | MODIFIER | c.-9G>A| |
S266 |
15 | BAA03g45700 | A03 | 21920581 | G | A | upstream_gene_variant | MODIFIER | c.-98C>T| |
S47 |