Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g40770 | A03 | 19067218 | G | A | missense_variant | MODERATE | c.59G>A|p.Arg20Lys |
S12 |
2 | BAA03g40770 | A03 | 19067780 | G | A | missense_variant | MODERATE | c.440G>A|p.Gly147Glu |
S260 |
3 | BAA03g40770 | A03 | 19067968 | G | A | missense_variant | MODERATE | c.524G>A|p.Gly175Glu |
S95 |
4 | BAA03g40770 | A03 | 19068695 | C | T | missense_variant | MODERATE | c.839C>T|p.Ser280Phe |
S134 |
5 | BAA03g40770 | A03 | 19070059 | C | T | missense_variant | MODERATE | c.1790C>T|p.Ser597Phe |
S1 S90 |
6 | BAA03g40770 | A03 | 19070379 | C | T | missense_variant | MODERATE | c.2110C>T|p.Pro704Ser |
S140 |
7 | BAA03g40770 | A03 | 19070409 | G | A | missense_variant | MODERATE | c.2140G>A|p.Glu714Lys |
S178 |
8 | BAA03g40770 | A03 | 19071535 | G | A | missense_variant | MODERATE | c.2971G>A|p.Asp991Asn |
S234 |
9 | BAA03g40770 | A03 | 19071765 | G | A | missense_variant | MODERATE | c.3127G>A|p.Glu1043Lys |
S104 S52 |