"Ambry Genetics"[submitter] AND "DUS2"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3274018	NM_017803.5(DUS2):c.95T>C (p.Leu32Pro)	DUS2 (L32P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086206	NM_017803.5(DUS2):c.107C>T (p.Ala36Val)	DUS2 (A36V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517798	NM_017803.5(DUS2):c.125A>C (p.Glu42Ala)	DUS2 (E42A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533587	NM_017803.5(DUS2):c.161G>A (p.Arg54Lys)	DUS2 (R54K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284922	NM_017803.5(DUS2):c.302G>C (p.Arg101Thr)	DUS2 (R101T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086211	NM_017803.5(DUS2):c.428C>T (p.Thr143Ile)	DUS2 (T108I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086212	NM_017803.5(DUS2):c.511C>T (p.Arg171Trp)	DUS2 (R136W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513513	NM_017803.5(DUS2):c.541G>A (p.Ala181Thr)	DUS2 (A146T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509829	NM_017803.5(DUS2):c.559C>T (p.Arg187Trp)	DUS2 (R187W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317644	NM_017803.5(DUS2):c.569G>A (p.Arg190Gln)	DUS2 (R155Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086214	NM_017803.5(DUS2):c.659A>G (p.His220Arg)	DUS2 (H185R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518539	NM_017803.5(DUS2):c.731C>G (p.Ala244Gly)	DUS2 (A209G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469478	NM_017803.5(DUS2):c.751A>G (p.Ile251Val)	DUS2 (I251V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086215	NM_017803.5(DUS2):c.794A>G (p.Gln265Arg)	DUS2 (Q230R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344064	NM_017803.5(DUS2):c.812C>T (p.Ala271Val)	DUS2 (A271V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086216	NM_017803.5(DUS2):c.814G>A (p.Val272Met)	DUS2 (V237M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470226	NM_017803.5(DUS2):c.827A>G (p.Asn276Ser)	DUS2 (N241S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469971	NM_017803.5(DUS2):c.884C>T (p.Ser295Leu)	DUS2 (S295L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086217	NM_017803.5(DUS2):c.950G>A (p.Gly317Asp)	DUS2, LOC130059264 (G282D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086204	NM_017803.5(DUS2):c.1023G>C (p.Gln341His)	DUS2 (Q341H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086205	NM_017803.5(DUS2):c.1037C>T (p.Ala346Val)	DUS2 (A346V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401772	NM_017803.5(DUS2):c.1136G>A (p.Arg379Gln)	DUS2 (R379Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274021	NM_017803.5(DUS2):c.1156C>T (p.Pro386Ser)	DUS2 (P386S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592938	NM_017803.5(DUS2):c.1190G>A (p.Arg397His)	DUS2 (R362H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298532	NM_017803.5(DUS2):c.1205T>A (p.Ile402Asn)	DUS2 (I367N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086208	NM_017803.5(DUS2):c.1289G>A (p.Cys430Tyr)	DUS2 (C430Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086209	NM_017803.5(DUS2):c.1352G>A (p.Arg451Gln)	DUS2 (R416Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086210	NM_017803.5(DUS2):c.1357A>T (p.Arg453Trp)	DUS2 (R453W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375370	NM_017803.5(DUS2):c.1427A>G (p.Lys476Arg)	DUS2 (K441R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3274022	NM_017803.5(DUS2):c.1445T>G (p.Leu482Trp)	DUS2 (L447W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 30