Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08530 | A05 | 4240738 | C | T | downstream_gene_variant | MODIFIER | c.*1393G>A| |
S193 |
2 | BAA05g08530 | A05 | 4242224 | C | T | synonymous_variant | LOW | c.4179G>A|p.Leu1393Leu |
S71 |
3 | BAA05g08530 | A05 | 4242347 | C | T | stop_gained | HIGH | c.4056G>A|p.Trp1352* |
S271 |
4 | BAA05g08530 | A05 | 4242999 | G | A | synonymous_variant | LOW | c.3573C>T|p.His1191His |
S308 |
5 | BAA05g08530 | A05 | 4244329 | C | T | missense_variant | MODERATE | c.2567G>A|p.Gly856Glu |
S208 S93 |
6 | BAA05g08530 | A05 | 4244334 | G | A | synonymous_variant | LOW | c.2562C>T|p.Ile854Ile |
S134 |
7 | BAA05g08530 | A05 | 4245672 | C | T | missense_variant | MODERATE | c.1813G>A|p.Val605Met |
S10 |
8 | BAA05g08530 | A05 | 4246451 | G | A | synonymous_variant | LOW | c.1173C>T|p.Leu391Leu |
S41 |
9 | BAA05g08530 | A05 | 4248064 | C | T | missense_variant | MODERATE | c.68G>A|p.Arg23Lys |
S107 |
10 | BAA05g08530 | A05 | 4248098 | C | T | missense_variant | MODERATE | c.34G>A|p.Glu12Lys |
S292 |
11 | BAA05g08530 | A05 | 4252526 | C | T | upstream_gene_variant | MODIFIER | c.-4395G>A| |
S289 S290 |