SLX9[gene] and "single gene"[properties] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3166223	NM_058190.4(SLX9):c.56A>G (p.Lys19Arg)	SLX9 (K19R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3166225	NM_058190.4(SLX9):c.59G>A (p.Gly20Glu)	SLX9 (G20E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590122	NM_058190.4(SLX9):c.88G>A (p.Ala30Thr)	SLX9 (A30T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3166209	NM_058190.4(SLX9):c.100A>C (p.Thr34Pro)	SLX9 (T34P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3166210	NM_058190.4(SLX9):c.136G>A (p.Ala46Thr)	SLX9 (A46T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3166211	NM_058190.4(SLX9):c.198G>C (p.Lys66Asn)	SLX9 (K66N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3166212	NM_058190.4(SLX9):c.211G>A (p.Val71Met)	SLX9 (V71M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3166213	NM_058190.4(SLX9):c.301G>A (p.Val101Ile)	SLX9 (V101I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3166214	NM_058190.4(SLX9):c.314A>G (p.Lys105Arg)	SLX9 (K90R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3166215	NM_058190.4(SLX9):c.335G>A (p.Arg112His)	SLX9 (R112H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166216	NM_058190.4(SLX9):c.397C>T (p.Arg133Trp)	SLX9 (R133W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166217	NM_058190.4(SLX9):c.413C>T (p.Thr138Met)	SLX9 (T138M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525128	NM_058190.4(SLX9):c.457G>A (p.Glu153Lys)	SLX9 (E138K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166218	NM_058190.4(SLX9):c.487C>T (p.Arg163Cys)	SLX9 (R148C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166219	NM_058190.4(SLX9):c.496C>T (p.Arg166Cys)	SLX9 (R59C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166220	NM_058190.4(SLX9):c.505G>A (p.Glu169Lys)	SLX9 (E154K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458291	NM_058190.4(SLX9):c.509G>A (p.Ser170Asn)	SLX9 (S154N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3166221	NM_058190.4(SLX9):c.511A>G (p.Asn171Asp)	SLX9 (N63D +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507509	NM_058190.4(SLX9):c.520C>T (p.Arg174Trp)	SLX9 (R66W +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3320620	NM_058190.4(SLX9):c.550G>A (p.Ala184Thr)	SLX9 (A168T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3166222	NM_058190.4(SLX9):c.563A>T (p.Gln188Leu)	SLX9 (Q172L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3166224	NM_058190.4(SLX9):c.587G>A (p.Arg196Gln)	SLX9 (R173Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166226	NM_058190.4(SLX9):c.617A>G (p.Tyr206Cys)	SLX9 (Y206C +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166227	NM_058190.4(SLX9):c.658C>T (p.Arg220Trp)	SLX9 (R182W +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166228	NM_058190.4(SLX9):c.659G>T (p.Arg220Leu)	SLX9 (R197L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166229	NM_058190.4(SLX9):c.686A>C (p.Gln229Pro)	SLX9 (Q229P +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 26