"Ambry Genetics"[submitter] AND "CRY2"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2476083	NM_021117.3(CRY2):c.22T>C (p.Tyr8His)	CRY2 (Y8H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296003	NM_021117.5(CRY2):c.11C>G (p.Thr4Ser)	CRY2 (T4S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077690	NM_021117.5(CRY2):c.41C>A (p.Ala14Glu)	CRY2 (A14E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482860	NM_021117.5(CRY2):c.41C>T (p.Ala14Val)	CRY2 (A14V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269643	NM_021117.5(CRY2):c.46G>C (p.Ala16Pro)	CRY2 (A16P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077691	NM_021117.5(CRY2):c.60C>G (p.Asp20Glu)	CRY2 (D20E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252996	NM_021117.5(CRY2):c.161A>G (p.Tyr54Cys)	CRY2 (Y54C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269642	NM_021117.5(CRY2):c.335T>C (p.Val112Ala)	CRY2 (V51A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524135	NM_021117.5(CRY2):c.382C>T (p.Arg128Trp)	CRY2 (R128W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364730	NM_021117.5(CRY2):c.433A>G (p.Thr145Ala)	CRY2 (T84A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342764	NM_021117.5(CRY2):c.434C>T (p.Thr145Met)	CRY2 (T145M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408612	NM_021117.5(CRY2):c.455A>G (p.Tyr152Cys)	CRY2 (Y91C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461882	NM_021117.5(CRY2):c.511C>T (p.Arg171Cys)	CRY2, LOC121832791 (R171C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269641	NM_021117.5(CRY2):c.535A>C (p.Met179Leu)	CRY2, LOC121832791 (M118L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077697	NM_021117.5(CRY2):c.598G>A (p.Glu200Lys)	CRY2, LOC121832791 (E200K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077698	NM_021117.5(CRY2):c.670C>A (p.Leu224Ile)	CRY2, LOC121832791 (L163I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293735	NM_021117.5(CRY2):c.733G>A (p.Glu245Lys)	CRY2, LOC121832791 (E245K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077699	NM_021117.5(CRY2):c.758A>G (p.Tyr253Cys)	CRY2 (Y192C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296569	NM_021117.5(CRY2):c.779C>T (p.Ala260Val)	CRY2 (A260V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412210	NM_021117.5(CRY2):c.856T>C (p.Tyr286His)	CRY2 (Y225H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342690	NM_021117.5(CRY2):c.859C>T (p.Arg287Cys)	CRY2 (R226C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254247	NM_021117.5(CRY2):c.955G>A (p.Ala319Thr)	CRY2 (A258T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530561	NM_021117.5(CRY2):c.995C>T (p.Pro332Leu)	CRY2 (P271L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610639	NM_021117.5(CRY2):c.1034C>T (p.Ala345Val)	CRY2 (A345V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607425	NM_021117.5(CRY2):c.1052A>G (p.Glu351Gly)	CRY2 (E290G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538100	NM_021117.5(CRY2):c.1126G>C (p.Ala376Pro)	CRY2 (A315P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077692	NM_021117.5(CRY2):c.1459C>T (p.Arg487Trp)	CRY2 (R487W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365225	NM_021117.5(CRY2):c.1468G>A (p.Val490Ile)	CRY2 (V490I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077693	NM_021117.5(CRY2):c.1480G>C (p.Glu494Gln)	CRY2 (E433Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461359	NM_021117.5(CRY2):c.1541G>A (p.Arg514Gln)	CRY2 (R453Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077694	NM_021117.5(CRY2):c.1558G>A (p.Ala520Thr)	CRY2 (A459T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077696	NM_021117.5(CRY2):c.1711G>C (p.Gly571Arg)	CRY2 (G571R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 32