Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g28960 | A03 | 13448728 | C | T | synonymous_variant | LOW | c.2469G>A|p.Lys823Lys |
S238 |
2 | BAA03g28960 | A03 | 13449688 | G | A | synonymous_variant | LOW | c.1860C>T|p.Ile620Ile |
S33 |
3 | BAA03g28960 | A03 | 13449733 | C | T | synonymous_variant | LOW | c.1815G>A|p.Gln605Gln |
S166 |
4 | BAA03g28960 | A03 | 13449881 | G | A | missense_variant | MODERATE | c.1667C>T|p.Thr556Ile |
S13 |
5 | BAA03g28960 | A03 | 13449909 | C | T | missense_variant | MODERATE | c.1639G>A|p.Gly547Ser |
S81 S85 |
6 | BAA03g28960 | A03 | 13449935 | G | A | missense_variant | MODERATE | c.1613C>T|p.Pro538Leu |
S186 |
7 | BAA03g28960 | A03 | 13450181 | C | T | synonymous_variant | LOW | c.1449G>A|p.Glu483Glu |
S304 |
8 | BAA03g28960 | A03 | 13450419 | G | A | stop_gained | HIGH | c.1312C>T|p.Gln438* |
S211 S227 |
9 | BAA03g28960 | A03 | 13450422 | C | T | missense_variant | MODERATE | c.1309G>A|p.Val437Met |
S28 |
10 | BAA03g28960 | A03 | 13450483 | C | T | synonymous_variant | LOW | c.1248G>A|p.Pro416Pro |
S207 |
11 | BAA03g28960 | A03 | 13451266 | C | T | missense_variant | MODERATE | c.721G>A|p.Ala241Thr |
S195 |
12 | BAA03g28960 | A03 | 13451921 | C | T | synonymous_variant | LOW | c.132G>A|p.Lys44Lys |
S32 |
13 | BAA03g28960 | A03 | 13453530 | C | T | upstream_gene_variant | MODIFIER | c.-1402G>A| |
S275 |
14 | BAA03g28960 | A03 | 13455835 | G | A | upstream_gene_variant | MODIFIER | c.-3707C>T| |
S233 |
15 | BAA03g28960 | A03 | 13456520 | C | T | upstream_gene_variant | MODIFIER | c.-4392G>A| |
S132 S137 S215 S89 |
16 | BAA03g28960 | A03 | 13456637 | C | T | upstream_gene_variant | MODIFIER | c.-4509G>A| |
S187 |