| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.79559458G>T | CA5574231 | SFTPA2 | c.26C>A (p.Thr9Asn) c.71C>A (p.Thr24Asn) c.77C>A (p.Thr26Asn) c.56C>A (p.Thr19Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.79559458G>C | CA5574232 | SFTPA2 | c.26C>G (p.Thr9Ser) c.71C>G (p.Thr24Ser) c.77C>G (p.Thr26Ser) c.56C>G (p.Thr19Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |