"PreventionGenetics, part of Exact Sciences"[submitter] AND "CCNL2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043139	NM_030937.6(CCNL2):c.*4G>A	CCNL2	Single nucleotide variant (3 prime UTR variant +1 more)	CCNL2-related condition	GBenign
Select item 3053233	NM_030937.6(CCNL2):c.990T>C (p.Ser330=)	CCNL2	Single nucleotide variant (synonymous variant +1 more)	CCNL2-related condition	GLikely benign
Select item 3060913	NM_030937.6(CCNL2):c.981G>A (p.Ser327=)	CCNL2	Single nucleotide variant (synonymous variant +1 more)	CCNL2-related condition	GLikely benign
Select item 3048068	NM_030937.6(CCNL2):c.474-6del	CCNL2	Deletion (5 prime UTR variant +1 more)	CCNL2-related condition	GLikely benign
Select item 3048381	NM_030937.6(CCNL2):c.473+10_473+13del	CCNL2	Microsatellite (intron variant)	CCNL2-related condition	GLikely benign
Select item 3033974	NM_030937.6(CCNL2):c.201C>T (p.Ser67=)	CCNL2, LOC129929121	Single nucleotide variant (synonymous variant +2 more)	CCNL2-related condition	GLikely benign
Select item 3058762	NM_030937.6(CCNL2):c.120G>A (p.Arg40=)	CCNL2, LOC129929121	Single nucleotide variant (synonymous variant +2 more)	CCNL2-related condition	GLikely benign
Select item 3052965	NM_030937.6(CCNL2):c.74C>G (p.Ser25Cys)	CCNL2 (S25C)	Single nucleotide variant (missense variant +2 more)	CCNL2-related condition	GLikely benign

ClinVar