Allele Registry

Chr	Mutation (hg38)	CAid	Linkouts
2	g.203870597_203875386del	CA915942297	ClinVar
2	g.203874116C>T	CA63790167	dbSNP
2	g.203874132G>T	CA539149823	gnomAD
2	g.203874135A>T	CA539149824	gnomAD
2	g.203874142G>A	CA763556320
2	g.203874146G>C	CA63790169	dbSNP gnomAD
2	g.203874146G>T	CA63790175	dbSNP
2	g.203874152A>G	CA63790185	dbSNP
2	g.203874155C>T	CA63790189	dbSNP gnomAD COSMIC
2	g.203874161C>G	CA63790190	dbSNP gnomAD
2	g.203874165T>C	CA63790192	dbSNP gnomAD
2	g.203874168A>G	CA539149825	gnomAD
2	g.203874170T>G	CA539149826	gnomAD
2	g.203874172C>T	CA63790204	dbSNP
2	g.203874175C>T	CA63790241	dbSNP
2	g.203874178_203874180del	CA763556335
2	g.203874177C>T	CA63790243	dbSNP gnomAD
2	g.203874180C>G	CA763556340
2	g.203874182A>G	CA63790248	dbSNP gnomAD
2	g.203874195C>T	CA63790252	dbSNP
2	g.203874196G>A	CA11297605	ClinVar dbSNP gnomAD
2	g.203874212A>G	CA763556356
2	g.203874214A>G	CA539149827	gnomAD
2	g.203874215G>A	CA11292058	dbSNP gnomAD

Number of alleles fetched