Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.37714662T>C | CA10024311 | KCNJ6 | c.495A>G (p.Pro165=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.37714662T>A | CA512334977 | KCNJ6 | c.495A>T (p.Pro165=) | dbSNP gnomAD v4 COSMIC |
21 | g.37714662T>G | CA512334974 | KCNJ6 | c.495A>C (p.Pro165=) | dbSNP |
21 | g.37714662T= | CA2388599240 | KCNJ6 | c.495A= (p.Pro165=) | dbSNP |