| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.215420652T>C | CA2095210 | FN1 | c.1675+21A>G (n.1675+21A>G) n.598+21A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.215420652T>A | CA1327366901 | FN1 | c.1675+21A>T (n.1675+21A>T) n.598+21A>T | dbSNP |
| 2 | g.215420652T= | CA1327366900 | FN1 | c.1675+21A= (n.1675+21A=) n.598+21A= | dbSNP |