Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.10413073G>ACA117400MKKSc.442C>T (p.Gln148Ter)
n.459-373C>T
n.364-4270C>T
n.347-4270C>T
 ClinVar dbSNP gnomAD v4
20g.10413073G=CA2349780946MKKSc.442C= (p.Gln148=)
n.459-373C=
n.364-4270C=
n.347-4270C=
 dbSNP

Number of alleles fetched