Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17110 | A09 | 10162624 | G | A | intron_variant | MODIFIER | c.71-38G>A| |
S202 |
2 | BAA09g17110 | A09 | 10162707 | C | T | missense_variant | MODERATE | c.116C>T|p.Pro39Leu |
S62 |
3 | BAA09g17110 | A09 | 10162883 | G | A | synonymous_variant | LOW | c.222G>A|p.Glu74Glu |
S140 S168 S219 S279 S64 S72 |
4 | BAA09g17110 | A09 | 10162978 | C | T | missense_variant | MODERATE | c.317C>T|p.Thr106Ile |
S115 |
5 | BAA09g17110 | A09 | 10162988 | C | T | synonymous_variant | LOW | c.327C>T|p.Leu109Leu |
S41 |
6 | BAA09g17110 | A09 | 10163712 | G | A | synonymous_variant | LOW | c.969G>A|p.Lys323Lys |
S8 |
7 | BAA09g17110 | A09 | 10164099 | C | T | missense_variant | MODERATE | c.1145C>T|p.Ser382Phe |
S76 |
8 | BAA09g17110 | A09 | 10164857 | G | A | downstream_gene_variant | MODIFIER | c.*115G>A| |
S156 |
9 | BAA09g17110 | A09 | 10165976 | G | A | downstream_gene_variant | MODIFIER | c.*1234G>A| |
S291 |
10 | BAA09g17110 | A09 | 10166035 | C | T | downstream_gene_variant | MODIFIER | c.*1293C>T| |
S135 |
11 | BAA09g17110 | A09 | 10166142 | G | A | downstream_gene_variant | MODIFIER | c.*1400G>A| |
S264 S56 |
12 | BAA09g17110 | A09 | 10166662 | C | T | downstream_gene_variant | MODIFIER | c.*1920C>T| |
S305 |
13 | BAA09g17110 | A09 | 10168910 | C | T | downstream_gene_variant | MODIFIER | c.*4168C>T| |
S135 |
14 | BAA09g17110 | A09 | 10168930 | C | T | downstream_gene_variant | MODIFIER | c.*4188C>T| |
S118 |
15 | BAA09g17110 | A09 | 10169386 | G | A | downstream_gene_variant | MODIFIER | c.*4644G>A| |
S178 |