Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02710 | A01 | 1257242 | G | A | missense_variant | MODERATE | c.314G>A|p.Gly105Glu |
S232 |
2 | BAA01g02710 | A01 | 1257446 | G | A | missense_variant | MODERATE | c.518G>A|p.Arg173Lys |
S108 |
3 | BAA01g02710 | A01 | 1257806 | C | T | synonymous_variant | LOW | c.696C>T|p.Arg232Arg |
S48 |
4 | BAA01g02710 | A01 | 1258104 | G | A | missense_variant | MODERATE | c.994G>A|p.Gly332Arg |
S272 |
5 | BAA01g02710 | A01 | 1258152 | G | A | missense_variant | MODERATE | c.1042G>A|p.Asp348Asn |
S224 |
6 | BAA01g02710 | A01 | 1258342 | G | A | missense_variant | MODERATE | c.1232G>A|p.Gly411Asp |
S60 |
7 | BAA01g02710 | A01 | 1258943 | C | T | missense_variant | MODERATE | c.1739C>T|p.Thr580Ile |
S192 |
8 | BAA01g02710 | A01 | 1258965 | C | T | synonymous_variant | LOW | c.1761C>T|p.Asn587Asn |
S182 |
9 | BAA01g02710 | A01 | 1259323 | C | T | missense_variant | MODERATE | c.2039C>T|p.Ser680Phe |
S129 |
10 | BAA01g02710 | A01 | 1260208 | C | T | missense_variant | MODERATE | c.2924C>T|p.Ser975Phe |
S189 |
11 | BAA01g02710 | A01 | 1260498 | G | A | missense_variant | MODERATE | c.3214G>A|p.Glu1072Lys |
S251 |
12 | BAA01g02710 | A01 | 1261667 | G | A | stop_gained | HIGH | c.4206G>A|p.Trp1402* |
S256 |