"Ambry Genetics"[submitter] AND "LRRC4C"[gene] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3120798	NM_001258419.2(LRRC4C):c.1810C>T (p.Pro604Ser)	LRRC4C (P604S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120797	NM_001258419.2(LRRC4C):c.1771G>A (p.Glu591Lys)	LRRC4C (E591K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328948	NM_001258419.2(LRRC4C):c.1732G>A (p.Asp578Asn)	LRRC4C (D578N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349145	NM_001258419.2(LRRC4C):c.1727C>T (p.Thr576Met)	LRRC4C (T576M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120796	NM_001258419.2(LRRC4C):c.1447G>A (p.Asp483Asn)	LRRC4C (D483N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476384	NM_001258419.2(LRRC4C):c.1438C>T (p.Pro480Ser)	LRRC4C (P480S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120795	NM_001258419.2(LRRC4C):c.1418A>T (p.Asp473Val)	LRRC4C (D473V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3291684	NM_001258419.2(LRRC4C):c.1393T>C (p.Ser465Pro)	LRRC4C (S465P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509085	NM_001258419.2(LRRC4C):c.1337C>T (p.Ala446Val)	LRRC4C (A446V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467495	NM_001258419.2(LRRC4C):c.1229C>T (p.Thr410Met)	LRRC4C (T410M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120794	NM_001258419.2(LRRC4C):c.1205G>A (p.Arg402Gln)	LRRC4C (R402Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379427	NM_001258419.2(LRRC4C):c.1193C>T (p.Ala398Val)	LRRC4C (A398V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3291686	NM_001258419.2(LRRC4C):c.1093G>A (p.Val365Ile)	LRRC4C (V365I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469405	NM_001258419.2(LRRC4C):c.1091A>G (p.Asn364Ser)	LRRC4C (N364S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120805	NM_001258419.2(LRRC4C):c.965C>T (p.Ser322Leu)	LRRC4C (S322L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120804	NM_001258419.2(LRRC4C):c.863C>T (p.Thr288Ile)	LRRC4C (T288I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120803	NM_001258419.2(LRRC4C):c.823G>A (p.Ala275Thr)	LRRC4C (A275T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120802	NM_001258419.2(LRRC4C):c.779G>A (p.Arg260Gln)	LRRC4C (R260Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208034	NM_001258419.2(LRRC4C):c.766C>A (p.Gln256Lys)	LRRC4C (Q256K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470476	NM_001258419.2(LRRC4C):c.730C>T (p.His244Tyr)	LRRC4C (H244Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314873	NM_001258419.2(LRRC4C):c.698C>A (p.Ala233Asp)	LRRC4C (A233D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2245764	NM_001258419.2(LRRC4C):c.698C>T (p.Ala233Val)	LRRC4C (A233V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473888	NM_001258419.2(LRRC4C):c.676C>A (p.Leu226Ile)	LRRC4C (L226I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120801	NM_001258419.2(LRRC4C):c.494C>T (p.Ser165Phe)	LRRC4C (S165F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120800	NM_001258419.2(LRRC4C):c.474C>A (p.Asn158Lys)	LRRC4C (N158K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120799	NM_001258419.2(LRRC4C):c.415A>G (p.Ile139Val)	LRRC4C (I139V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373098	NM_001258419.2(LRRC4C):c.404G>A (p.Arg135His)	LRRC4C (R135H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476666	NM_001258419.2(LRRC4C):c.220A>G (p.Ile74Val)	LRRC4C (I74V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3120793	NM_001258419.2(LRRC4C):c.102A>T (p.Gln34His)	LRRC4C (Q34H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 29