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| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94761900C>T | CA10602359 | n.932-13158C>T (p.=) | ClinVar dbSNP gnomAD | |
| 10 | g.94761900C>A | CA10576167 | n.932-13158C>A (p.=) | ClinVar dbSNP |