Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g02660 | A03 | 1169955 | C | T | synonymous_variant | LOW | c.303C>T|p.Phe101Phe |
S76 |
2 | BAA03g02660 | A03 | 1169983 | C | T | missense_variant | MODERATE | c.331C>T|p.Leu111Phe |
S79 S91 |
3 | BAA03g02660 | A03 | 1170019 | C | T | missense_variant | MODERATE | c.367C>T|p.Arg123Trp |
S283 |
4 | BAA03g02660 | A03 | 1170248 | G | A | missense_variant | MODERATE | c.596G>A|p.Arg199Gln |
S274 |
5 | BAA03g02660 | A03 | 1170505 | G | A | missense_variant | MODERATE | c.853G>A|p.Asp285Asn |
S206 S26 |
6 | BAA03g02660 | A03 | 1170763 | G | A | missense_variant | MODERATE | c.1111G>A|p.Ala371Thr |
S76 |
7 | BAA03g02660 | A03 | 1170886 | C | T | missense_variant | MODERATE | c.1234C>T|p.Pro412Ser |
S164 |
8 | BAA03g02660 | A03 | 1170913 | G | A | missense_variant | MODERATE | c.1261G>A|p.Val421Ile |
S150 |