"Ambry Genetics"[submitter] AND "UNC5D"[gene] - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3186641	NM_080872.4(UNC5D):c.23C>G (p.Ala8Gly)	UNC5D (A8G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2609375	NM_080872.4(UNC5D):c.40G>A (p.Ala14Thr)	UNC5D (A14T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186646	NM_080872.4(UNC5D):c.43C>T (p.Arg15Cys)	UNC5D (R15C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330491	NM_080872.4(UNC5D):c.91G>T (p.Ala31Ser)	UNC5D (A31S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595957	NM_080872.4(UNC5D):c.130G>A (p.Glu44Lys)	UNC5D (E39K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393271	NM_080872.4(UNC5D):c.177G>T (p.Glu59Asp)	UNC5D (E59D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186638	NM_080872.4(UNC5D):c.211A>G (p.Ile71Val)	UNC5D (I66V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407947	NM_080872.4(UNC5D):c.230C>T (p.Ala77Val)	UNC5D (A72V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186643	NM_080872.4(UNC5D):c.265G>A (p.Gly89Ser)	UNC5D (G84S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553464	NM_080872.4(UNC5D):c.286G>A (p.Glu96Lys)	UNC5D (E96K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186644	NM_080872.4(UNC5D):c.332T>G (p.Val111Gly)	UNC5D (V106G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3331073	NM_080872.4(UNC5D):c.335G>A (p.Arg112His)	UNC5D (R107H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186645	NM_080872.4(UNC5D):c.388G>A (p.Glu130Lys)	UNC5D (E125K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531611	NM_080872.4(UNC5D):c.511C>T (p.Pro171Ser)	UNC5D (P171S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373868	NM_080872.4(UNC5D):c.676T>G (p.Ser226Ala)	LOC101929550, UNC5D (S221A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607492	NM_080872.4(UNC5D):c.695T>G (p.Met232Arg)	LOC101929550, UNC5D (M227R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186647	NM_080872.4(UNC5D):c.713C>T (p.Ala238Val)	LOC101929550, UNC5D (A233V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608240	NM_080872.4(UNC5D):c.1052C>A (p.Ser351Tyr)	LOC101929550, UNC5D (S346Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535506	NM_080872.4(UNC5D):c.1118G>A (p.Ser373Asn)	UNC5D (S373N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186631	NM_080872.4(UNC5D):c.1135G>A (p.Asp379Asn)	UNC5D (D374N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186632	NM_080872.4(UNC5D):c.1160G>A (p.Gly387Asp)	UNC5D (G320D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186633	NM_080872.4(UNC5D):c.1171G>A (p.Val391Met)	UNC5D (V386M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186634	NM_080872.4(UNC5D):c.1354C>T (p.Arg452Trp)	UNC5D (R385W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3331072	NM_080872.4(UNC5D):c.1355G>A (p.Arg452Gln)	UNC5D (R452Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186635	NM_080872.4(UNC5D):c.1366G>A (p.Gly456Arg)	UNC5D (G451R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507715	NM_080872.4(UNC5D):c.1639G>A (p.Val547Ile)	UNC5D (V542I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186636	NM_080872.4(UNC5D):c.1841C>T (p.Thr614Ile)	UNC5D (T547I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272143	NM_080872.4(UNC5D):c.1913G>C (p.Arg638Thr)	UNC5D (R633T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612141	NM_080872.4(UNC5D):c.1915A>G (p.Thr639Ala)	UNC5D (T572A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518969	NM_080872.4(UNC5D):c.1967C>A (p.Ser656Tyr)	UNC5D (S656Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236844	NM_080872.4(UNC5D):c.2015G>A (p.Ser672Asn)	UNC5D (S605N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186637	NM_080872.4(UNC5D):c.2077G>A (p.Val693Met)	UNC5D (V693M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516723	NM_080872.4(UNC5D):c.2095A>C (p.Met699Leu)	UNC5D (M632L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272406	NM_080872.4(UNC5D):c.2107T>C (p.Ser703Pro)	UNC5D (S636P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484883	NM_080872.4(UNC5D):c.2231A>G (p.Lys744Arg)	UNC5D (K677R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186639	NM_080872.4(UNC5D):c.2263C>G (p.Leu755Val)	UNC5D (L750V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403671	NM_080872.4(UNC5D):c.2329C>T (p.Arg777Cys)	UNC5D (R772C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3186642	NM_080872.4(UNC5D):c.2486G>A (p.Arg829Gln)	UNC5D (R824Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3331074	NM_080872.4(UNC5D):c.2566T>C (p.Ser856Pro)	UNC5D (S789P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484280	NM_080872.4(UNC5D):c.2579G>A (p.Arg860Gln)	UNC5D (R855Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617424	NM_080872.4(UNC5D):c.2804T>G (p.Ile935Ser)	UNC5D (I935S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 41