Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.128853831A>T | CA10586206 | FLNC,FLNC-AS1 | c.6478A>T (p.Ile2160Phe) c.6379A>T (p.Ile2127Phe) n.103-434T>A | ClinVar dbSNP |
7 | g.128853831A= | CA1742578224 | FLNC,FLNC-AS1 | c.6478A= (p.Ile2160=) c.6379A= (p.Ile2127=) n.103-434T= | dbSNP |