CRELD2[gene] and "single gene"[properties] - ClinVar

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Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3269489	NM_024324.5(CRELD2):c.97C>T (p.Arg33Trp)	CRELD2 (R33W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542236	NM_024324.5(CRELD2):c.97C>G (p.Arg33Gly)	CRELD2 (R33G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380418	NM_024324.5(CRELD2):c.98G>A (p.Arg33Gln)	CRELD2 (R33Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077390	NM_024324.5(CRELD2):c.112G>C (p.Val38Leu)	CRELD2 (V38L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475960	NM_024324.5(CRELD2):c.214G>A (p.Glu72Lys)	CRELD2 (E72K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225925	NM_024324.5(CRELD2):c.275A>G (p.Gln92Arg)	CRELD2 (Q92R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207316	NM_024324.5(CRELD2):c.276G>C (p.Gln92His)	CRELD2 (Q92H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553249	NM_024324.5(CRELD2):c.354G>T (p.Trp118Cys)	CRELD2 (W118C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474938	NM_024324.5(CRELD2):c.400G>T (p.Gly134Cys)	CRELD2 (G134C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377103	NM_024324.5(CRELD2):c.400G>A (p.Gly134Ser)	CRELD2 (G134S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308340	NM_024324.5(CRELD2):c.430T>C (p.Ser144Pro)	CRELD2 (S144P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077392	NM_024324.5(CRELD2):c.448G>A (p.Gly150Arg)	CRELD2 (G150R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269485	NM_024324.5(CRELD2):c.466G>A (p.Gly156Arg)	CRELD2 (G156R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 777763	NM_024324.5(CRELD2):c.486C>T (p.Gly162=)	CRELD2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3269488	NM_024324.5(CRELD2):c.500G>A (p.Arg167Gln)	CRELD2 (R167Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3077393	NM_024324.5(CRELD2):c.566G>A (p.Arg189Gln)	CRELD2 (R189Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077395	NM_024324.5(CRELD2):c.569A>G (p.Asn190Ser)	CRELD2 (N190S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077396	NM_024324.5(CRELD2):c.582C>A (p.Ser194Arg)	CRELD2 (S194R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 770820	NM_024324.5(CRELD2):c.593-322_593-286del	CRELD2	Deletion (splice acceptor variant +1 more)	not provided	GBenign
Select item 2378473	NM_024324.5(CRELD2):c.593-294C>G	CRELD2 (S205C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2275730	NM_024324.5(CRELD2):c.593-244G>A	CRELD2 (A222T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077397	NM_024324.5(CRELD2):c.593-241T>C	CRELD2 (W223R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369509	NM_024324.5(CRELD2):c.593-222C>T	CRELD2 (T229M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215483	NM_024324.5(CRELD2):c.593-208G>T	CRELD2 (G234C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459029	NM_024324.5(CRELD2):c.593-181G>T	CRELD2 (A243S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077398	NM_024324.5(CRELD2):c.620C>T (p.Ser207Leu)	CRELD2 (S207L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2653354	NM_024324.5(CRELD2):c.621G>A (p.Ser207=)	CRELD2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3077399	NM_024324.5(CRELD2):c.632A>G (p.Asn211Ser)	CRELD2 (N211S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602531	NM_024324.5(CRELD2):c.652G>A (p.Glu218Lys)	CRELD2 (E218K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077400	NM_024324.5(CRELD2):c.679G>A (p.Ala227Thr)	CRELD2 (A227T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536871	NM_024324.5(CRELD2):c.691G>A (p.Val231Met)	CRELD2 (V231M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 784426	NM_024324.5(CRELD2):c.708C>T (p.Ala236=)	CRELD2	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2595519	NM_024324.5(CRELD2):c.742A>G (p.Lys248Glu)	CRELD2 (K297E +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2653355	NM_024324.5(CRELD2):c.747C>T (p.Asn249=)	CRELD2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2260328	NM_024324.5(CRELD2):c.763A>G (p.Thr255Ala)	CRELD2 (T304A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2296459	NM_024324.5(CRELD2):c.764C>T (p.Thr255Met)	CRELD2 (T255M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3077401	NM_024324.5(CRELD2):c.769G>A (p.Glu257Lys)	CRELD2 (E257K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2209333	NM_024324.5(CRELD2):c.773A>C (p.Glu258Ala)	CRELD2 (E230A +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3077402	NM_024324.5(CRELD2):c.833T>C (p.Ile278Thr)	CRELD2 (I278T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3077389	NM_024324.5(CRELD2):c.863G>A (p.Cys288Tyr)	CRELD2 (C288Y +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2238539	NM_024324.5(CRELD2):c.1019A>T (p.Glu340Val)	CRELD2 (E389V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269487	NM_024324.5(CRELD2):c.1026A>C (p.Glu342Asp)	CRELD2 (E314D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235195	NM_024324.5(CRELD2):c.1028G>A (p.Ser343Asn)	CRELD2 (S343N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624322	NM_024324.5(CRELD2):c.1056C>A (p.Asp352Glu)	CRELD2 (D352E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 44