Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g42400 | A01 | 28169456 | C | T | missense_variant | MODERATE | c.1277G>A|p.Arg426His |
S107 |
2 | BAA01g42400 | A01 | 28169889 | C | T | missense_variant | MODERATE | c.844G>A|p.Asp282Asn |
S273 |
3 | BAA01g42400 | A01 | 28170288 | G | A | missense_variant | MODERATE | c.619C>T|p.Pro207Ser |
S105 S106 |
4 | BAA01g42400 | A01 | 28170357 | G | A | missense_variant | MODERATE | c.550C>T|p.Pro184Ser |
S218 |
5 | BAA01g42400 | A01 | 28170564 | G | A | synonymous_variant | LOW | c.420C>T|p.Ala140Ala |
S33 |
6 | BAA01g42400 | A01 | 28171411 | C | T | missense_variant | MODERATE | c.46G>A|p.Ala16Thr |
S205 |
7 | BAA01g42400 | A01 | 28171454 | C | T | start_lost | HIGH | c.3G>A|p.Met1? |
S282 |
8 | BAA01g42400 | A01 | 28174923 | C | T | upstream_gene_variant | MODIFIER | c.-3467G>A| |
S39 |
9 | BAA01g42400 | A01 | 28175557 | G | A | upstream_gene_variant | MODIFIER | c.-4101C>T| |
S2 |
10 | BAA01g42400 | A01 | 28175873 | G | A | upstream_gene_variant | MODIFIER | c.-4417C>T| |
S6 |
11 | BAA01g42400 | A01 | 28175941 | G | A | upstream_gene_variant | MODIFIER | c.-4485C>T| |
S217 S248 |