Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39670 | A01 | 26341171 | C | T | missense_variant | MODERATE | c.46C>T|p.Leu16Phe |
S266 |
2 | BAA01g39670 | A01 | 26341244 | C | T | missense_variant | MODERATE | c.119C>T|p.Ser40Phe |
S39 |
3 | BAA01g39670 | A01 | 26341356 | C | T | synonymous_variant | LOW | c.231C>T|p.Val77Val |
S62 |
4 | BAA01g39670 | A01 | 26341385 | C | T | missense_variant | MODERATE | c.260C>T|p.Ser87Phe |
S159 S243 |
5 | BAA01g39670 | A01 | 26341659 | C | T | synonymous_variant | LOW | c.534C>T|p.Ser178Ser |
S59 |
6 | BAA01g39670 | A01 | 26341999 | C | T | missense_variant | MODERATE | c.874C>T|p.Pro292Ser |
S161 |
7 | BAA01g39670 | A01 | 26342212 | C | T | synonymous_variant | LOW | c.1087C>T|p.Leu363Leu |
S293 |
8 | BAA01g39670 | A01 | 26342352 | C | T | synonymous_variant | LOW | c.1227C>T|p.Asn409Asn |
S234 |
9 | BAA01g39670 | A01 | 26342852 | C | T | missense_variant | MODERATE | c.1727C>T|p.Thr576Ile |
S166 |
10 | BAA01g39670 | A01 | 26343043 | C | T | synonymous_variant | LOW | c.1918C>T|p.Leu640Leu |
S63 |