Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.37714662T>CCA10024311KCNJ6c.495A>G (p.Pro165=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.37714662T>ACA512334977KCNJ6c.495A>T (p.Pro165=)
dbSNP gnomAD v4 COSMIC
21g.37714662T>GCA512334974KCNJ6c.495A>C (p.Pro165=)
dbSNP
21g.37714662T=CA2388599240KCNJ6c.495A= (p.Pro165=)
dbSNP

Number of alleles fetched