| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.42739895G>A | CA339947294 | CLDN19 | c.169C>T (p.Gln57Ter) | ClinVar dbSNP |
| 1 | g.42739895G>C | CA114956 | CLDN19 | c.169C>G (p.Gln57Glu) | ClinVar dbSNP |
| 1 | g.42739895G= | CA1141579751 | CLDN19 | c.169C= (p.Gln57=) | dbSNP |
| 1 | g.42739895G>T | CA339947295 | CLDN19 | c.169C>A (p.Gln57Lys) | dbSNP gnomAD v4 |