| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.58363582G>C | CA400339404 | RNF43 | c.394C>G (p.Arg132Gly) c.13C>G (p.Arg5Gly) n.11C>G c.271C>G (p.Arg91Gly) | dbSNP gnomAD v4 |
| 17 | g.58363582G>A | CA214568 | RNF43 | c.394C>T (p.Arg132Ter) c.13C>T (p.Arg5Ter) n.11C>T c.271C>T (p.Arg91Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
| 17 | g.58363582G>T | CA501058237 | RNF43 | c.394C>A (p.Arg132=) c.13C>A (p.Arg5=) n.11C>A c.271C>A (p.Arg91=) | dbSNP |