SCARA5[gene] and "single gene"[properties] - ClinVar

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Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3316401	NM_173833.6(SCARA5):c.1411C>T (p.Arg471Cys)	SCARA5 (R428C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316407	NM_173833.6(SCARA5):c.1372G>A (p.Asp458Asn)	SCARA5 (D190N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321510	NM_173833.6(SCARA5):c.1225T>C (p.Tyr409His)	SCARA5 (Y141H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158305	NM_173833.6(SCARA5):c.1202C>T (p.Pro401Leu)	SCARA5 (P133L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316408	NM_173833.6(SCARA5):c.1171A>G (p.Met391Val)	SCARA5 (M123V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316410	NM_173833.6(SCARA5):c.1169C>T (p.Pro390Leu)	SCARA5 (P347L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536225	NM_173833.6(SCARA5):c.830T>C (p.Leu277Pro)	SCARA5 (L234P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256813	NM_173833.6(SCARA5):c.799G>A (p.Val267Ile)	SCARA5 (V224I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158311	NM_173833.6(SCARA5):c.788G>C (p.Arg263Pro)	SCARA5 (R263P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2569834	NM_173833.6(SCARA5):c.778C>T (p.Arg260Cys)	SCARA5 (R217C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399452	NM_173833.6(SCARA5):c.772G>A (p.Asp258Asn)	SCARA5 (D258N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480395	NM_173833.6(SCARA5):c.746G>A (p.Arg249Gln)	SCARA5 (R206Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3158310	NM_173833.6(SCARA5):c.674G>A (p.Gly225Asp)	SCARA5 (G225D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2271820	NM_173833.6(SCARA5):c.619G>A (p.Asp207Asn)	SCARA5 (D164N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323047	NM_173833.6(SCARA5):c.602G>A (p.Arg201His)	SCARA5 (R201H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158309	NM_173833.6(SCARA5):c.567G>T (p.Gln189His)	SCARA5 (Q146H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226540	NM_173833.6(SCARA5):c.566A>G (p.Gln189Arg)	SCARA5 (Q146R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316406	NM_173833.6(SCARA5):c.553C>A (p.Leu185Ile)	SCARA5 (L142I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474579	NM_173833.6(SCARA5):c.518G>A (p.Arg173His)	SCARA5 (R173H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316404	NM_173833.6(SCARA5):c.512G>A (p.Arg171Gln)	SCARA5 (R128Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343091	NM_173833.6(SCARA5):c.487A>G (p.Thr163Ala)	SCARA5 (T163A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462592	NM_173833.6(SCARA5):c.473C>A (p.Ala158Glu)	SCARA5 (A115E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524719	NM_173833.6(SCARA5):c.443G>A (p.Arg148Gln)	SCARA5 (R105Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316403	NM_173833.6(SCARA5):c.433G>T (p.Ala145Ser)	SCARA5 (A102S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468310	NM_173833.6(SCARA5):c.433G>A (p.Ala145Thr)	SCARA5 (A102T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3158308	NM_173833.6(SCARA5):c.427G>A (p.Ala143Thr)	SCARA5 (A100T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319805	NM_173833.6(SCARA5):c.418C>A (p.Leu140Met)	SCARA5 (L140M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316409	NM_173833.6(SCARA5):c.391G>A (p.Ala131Thr)	SCARA5 (A88T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319273	NM_173833.6(SCARA5):c.371A>G (p.Gln124Arg)	SCARA5 (Q124R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216927	NM_173833.6(SCARA5):c.365C>T (p.Thr122Met)	SCARA5 (T122M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158307	NM_173833.6(SCARA5):c.361C>A (p.Leu121Met)	SCARA5 (L121M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3158306	NM_173833.6(SCARA5):c.289A>C (p.Asn97His)	SCARA5 (N54H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292110	NM_173833.6(SCARA5):c.287G>A (p.Arg96His)	SCARA5 (R96H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246454	NM_173833.6(SCARA5):c.229T>C (p.Phe77Leu)	SCARA5 (F77L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251850	NM_173833.6(SCARA5):c.224G>T (p.Gly75Val)	SCARA5 (G75V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361924	NM_173833.6(SCARA5):c.172C>G (p.Leu58Val)	SCARA5 (L58V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378414	NM_173833.6(SCARA5):c.145T>C (p.Cys49Arg)	SCARA5 (C49R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316400	NM_173833.6(SCARA5):c.131G>A (p.Arg44Gln)	SCARA5 (R44Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3316402	NM_173833.6(SCARA5):c.130C>T (p.Arg44Trp)	SCARA5 (R44W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2403058	NM_173833.6(SCARA5):c.128G>A (p.Arg43Gln)	SCARA5 (R43Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351029	NM_173833.6(SCARA5):c.71T>C (p.Phe24Ser)	SCARA5 (F24S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495617	NM_173833.6(SCARA5):c.46A>G (p.Thr16Ala)	SCARA5 (T16A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279523	NM_173833.6(SCARA5):c.31G>A (p.Val11Ile)	SCARA5 (V11I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291580	NM_173833.6(SCARA5):c.13G>A (p.Ala5Thr)	SCARA5 (A5T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363225	NM_173833.6(SCARA5):c.8A>G (p.Asn3Ser)	SCARA5 (N3S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 45