Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g59950 | A03 | 30134970 | C | T | downstream_gene_variant | MODIFIER | c.*116G>A| |
S172 S217 |
2 | BAA03g59950 | A03 | 30135495 | G | A | missense_variant | MODERATE | c.2740C>T|p.Leu914Phe |
S115 |
3 | BAA03g59950 | A03 | 30136253 | C | T | missense_variant | MODERATE | c.2152G>A|p.Asp718Asn |
S136 |
4 | BAA03g59950 | A03 | 30136440 | C | T | missense_variant | MODERATE | c.2047G>A|p.Ala683Thr |
S293 |
5 | BAA03g59950 | A03 | 30136776 | G | A | missense_variant | MODERATE | c.1795C>T|p.Leu599Phe |
S148 S210 |
6 | BAA03g59950 | A03 | 30136801 | G | A | synonymous_variant | LOW | c.1770C>T|p.Arg590Arg |
S275 |
7 | BAA03g59950 | A03 | 30138203 | C | T | missense_variant&splice_region_variant | MODERATE | c.1016G>A|p.Arg339Lys |
S184 |
8 | BAA03g59950 | A03 | 30138301 | C | T | synonymous_variant | LOW | c.918G>A|p.Glu306Glu |
S33 |
9 | BAA03g59950 | A03 | 30138530 | C | T | missense_variant | MODERATE | c.757G>A|p.Val253Met |
S76 |
10 | BAA03g59950 | A03 | 30139253 | C | T | missense_variant | MODERATE | c.514G>A|p.Asp172Asn |
S297 |
11 | BAA03g59950 | A03 | 30139290 | C | T | synonymous_variant | LOW | c.477G>A|p.Leu159Leu |
S297 |
12 | BAA03g59950 | A03 | 30139399 | G | A | missense_variant | MODERATE | c.368C>T|p.Ala123Val |
S183 S198 |