"Ambry Genetics"[submitter] AND "DDR2"[gene] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2496217	NM_006182.4(DDR2):c.85A>G (p.Ile29Val)	DDR2 (I29V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2233040	NM_006182.4(DDR2):c.190G>T (p.Asp64Tyr)	DDR2 (D64Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2245313	NM_006182.4(DDR2):c.192C>A (p.Asp64Glu)	DDR2 (D64E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2234232	NM_006182.4(DDR2):c.274C>T (p.His92Tyr)	DDR2 (H92Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2305596	NM_006182.4(DDR2):c.431A>G (p.Asn144Ser)	DDR2 (N144S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3080830	NM_006182.4(DDR2):c.721G>A (p.Asp241Asn)	DDR2 (D241N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1412259	NM_006182.4(DDR2):c.832A>G (p.Ile278Val)	DDR2 (I278V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2277257	NM_006182.4(DDR2):c.918C>A (p.Phe306Leu)	DDR2 (F306L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2524499	NM_006182.4(DDR2):c.964C>T (p.Leu322Phe)	DDR2 (L322F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1896038	NM_006182.4(DDR2):c.979G>A (p.Val327Ile)	DDR2 (V327I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1001294	NM_006182.4(DDR2):c.1004C>T (p.Thr335Met)	DDR2 (T335M)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1041969	NM_006182.4(DDR2):c.1153A>T (p.Thr385Ser)	DDR2 (T385S)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1928315	NM_006182.4(DDR2):c.1170G>C (p.Met390Ile)	DDR2 (M390I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1224480	NM_006182.4(DDR2):c.1196G>A (p.Arg399Gln)	DDR2 (R399Q)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2213212	NM_006182.4(DDR2):c.1421T>A (p.Ile474Asn)	DDR2 (I474N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3080826	NM_006182.4(DDR2):c.1435C>T (p.Pro479Ser)	DDR2 (P479S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1023192	NM_006182.4(DDR2):c.1464A>G (p.Ile488Met)	DDR2 (I488M)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3080827	NM_006182.4(DDR2):c.1753A>G (p.Met585Val)	DDR2 (M585V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2302437	NM_006182.4(DDR2):c.1799A>G (p.Asn600Ser)	DDR2 (N600S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3271227	NM_006182.4(DDR2):c.2005C>T (p.His669Tyr)	DDR2 (H669Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3080828	NM_006182.4(DDR2):c.2007C>A (p.His669Gln)	DDR2 (H669Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2064816	NM_006182.4(DDR2):c.2012C>T (p.Pro671Leu)	DDR2 (P671L)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2327430	NM_006182.4(DDR2):c.2038C>G (p.Arg680Gly)	DDR2 (R680G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2181517	NM_006182.4(DDR2):c.2057A>G (p.Asn686Ser)	DDR2 (N686S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3080829	NM_006182.4(DDR2):c.2212G>A (p.Gly738Ser)	DDR2 (G738S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2074777	NM_006182.4(DDR2):c.2224C>T (p.Arg742Trp)	DDR2 (R742W)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2334169	NM_006182.4(DDR2):c.2368T>A (p.Ser790Thr)	DDR2 (S790T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334170	NM_006182.4(DDR2):c.2369C>A (p.Ser790Tyr)	DDR2 (S790Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 28