Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.154367844G>T | CA415248967 | FLNA | c.620C>A (p.Pro207Gln) c.539C>A (p.Pro180Gln) c.578C>A (p.Pro193Gln) | ClinVar dbSNP |
X | g.154367844G>A | CA256056 | FLNA | c.620C>T (p.Pro207Leu) c.539C>T (p.Pro180Leu) c.578C>T (p.Pro193Leu) | ClinVar dbSNP COSMIC COSMIC |
X | g.154367844G= | CA2466659042 | FLNA | c.620C= (p.Pro207=) c.539C= (p.Pro180=) c.578C= (p.Pro193=) | dbSNP |