"Ambry Genetics"[submitter] AND "CADM2"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3262913	NM_001167675.2(CADM2):c.203C>T (p.Pro68Leu)	CADM2, CADM2-AS2 (P52L +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2243247	NM_001167675.2(CADM2):c.344T>C (p.Leu115Ser)	CADM2 (L108S +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2261926	NM_001167675.2(CADM2):c.412A>T (p.Ile138Phe)	CADM2 (I122F +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136581	NM_001167675.2(CADM2):c.662C>T (p.Ala221Val)	CADM2 (A205V +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3262911	NM_001167675.2(CADM2):c.679A>G (p.Met227Val)	CADM2 (M177V +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3136582	NM_001167675.2(CADM2):c.684G>C (p.Gln228His)	CADM2 (Q212H +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3262912	NM_001167675.2(CADM2):c.704C>A (p.Thr235Lys)	CADM2 (T118K +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3262915	NM_001167675.2(CADM2):c.769T>G (p.Cys257Gly)	CADM2 (C160G +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261386	NM_001167675.2(CADM2):c.800C>T (p.Pro267Leu)	CADM2 (P221L +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263655	NM_001167675.2(CADM2):c.871A>T (p.Asn291Tyr)	CADM2 (N241Y +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326120	NM_001167675.2(CADM2):c.970+17565C>A	CADM2 (T331N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301719	NM_001167675.2(CADM2):c.970+17579A>G	CADM2 (T336A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516400	NM_001167675.2(CADM2):c.973C>T (p.Pro325Ser)	CADM2 (P208S +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3136580	NM_001167675.2(CADM2):c.1072G>C (p.Gly358Arg)	CADM2 (G261R +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311882	NM_001167675.2(CADM2):c.1193A>G (p.Glu398Gly)	CADM2 (E348G +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607000	NM_001167675.2(CADM2):c.1210A>G (p.Ile404Val)	CADM2 (I354V +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance