| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.49014710G>A | CA15223110 | FSHR | c.374+2779C>T (n.374+2779C>T) c.*153C>T (n.*153C>T) c.28C>T (p.Arg10Trp) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.49014710G= | CA1248779216 | FSHR | c.374+2779C= (n.374+2779C=) c.*153C= (n.*153C=) c.28C= (p.Arg10=) | dbSNP |