"GeneDx"[submitter] AND "CCND2-AS1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146024	GRCh38/hg38 12p13.33-13.31(chr12:45740-6945196)x3	ACRBP, ADIPOR2 +348 more	Copy number gain	See cases	GPathogenic
Select item 673833	NM_001759.3(CCND2):c.-608A>G	CCND2, CCND2-AS1	Single nucleotide variant	not provided	GBenign
Select item 678294	NM_001759.4(CCND2):c.-171C>T	CCND2, CCND2-AS1	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign
Select item 507367	NM_001759.4(CCND2):c.-36G>T	CCND2, CCND2-AS1	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GBenign
Select item 1806540	NM_001759.4(CCND2):c.100G>C (p.Glu34Gln)	CCND2, CCND2-AS1 (E34Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1280861	NM_001759.4(CCND2):c.114T>G (p.Leu38=)	CCND2, CCND2-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 3371289	NM_001759.4(CCND2):c.137G>C (p.Cys46Ser)	CCND2, CCND2-AS1 (C46S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1209058	NM_001759.4(CCND2):c.195+269A>C	CCND2, CCND2-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1204105	NM_001759.4(CCND2):c.196-104A>T	CCND2, CCND2-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1195560	NM_001759.4(CCND2):c.196-31G>C	CCND2, CCND2-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign