"Ambry Genetics"[submitter] AND "DAAM2"[gene] - ClinVar

Search results

Items: 90

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3270755	NM_001201427.2(DAAM2):c.7C>T (p.Pro3Ser)	DAAM2 (P3S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3036664	NM_001201427.2(DAAM2):c.11G>A (p.Arg4His)	DAAM2 (R4H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2596705	NM_001201427.2(DAAM2):c.11G>T (p.Arg4Leu)	DAAM2 (R4L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079860	NM_001201427.2(DAAM2):c.20G>A (p.Ser7Asn)	DAAM2 (S7N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079873	NM_001201427.2(DAAM2):c.82C>T (p.Arg28Trp)	DAAM2 (R28W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2330532	NM_001201427.2(DAAM2):c.208T>C (p.Phe70Leu)	DAAM2 (F70L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2402432	NM_001201427.2(DAAM2):c.313C>T (p.Arg105Cys)	DAAM2 (R105C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2322034	NM_001201427.2(DAAM2):c.412C>T (p.Arg138Trp)	DAAM2 (R138W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079871	NM_001201427.2(DAAM2):c.413G>A (p.Arg138Gln)	DAAM2 (R138Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2615758	NM_001201427.2(DAAM2):c.506G>C (p.Cys169Ser)	DAAM2 (C169S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2457770	NM_001201427.2(DAAM2):c.514C>T (p.Arg172Cys)	DAAM2 (R172C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2386126	NM_001201427.2(DAAM2):c.592C>T (p.Pro198Ser)	DAAM2 (P198S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079872	NM_001201427.2(DAAM2):c.625C>G (p.Arg209Gly)	DAAM2 (R209G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3270762	NM_001201427.2(DAAM2):c.699C>G (p.His233Gln)	DAAM2 (H233Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2599122	NM_001201427.2(DAAM2):c.740C>T (p.Ala247Val)	DAAM2 (A247V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2328247	NM_001201427.2(DAAM2):c.754C>T (p.Arg252Cys)	DAAM2 (R252C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2267156	NM_001201427.2(DAAM2):c.784C>G (p.Arg262Gly)	DAAM2 (R262G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2275295	NM_001201427.2(DAAM2):c.797G>A (p.Arg266Gln)	DAAM2 (R266Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2619402	NM_001201427.2(DAAM2):c.955C>T (p.His319Tyr)	DAAM2 (H319Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2361794	NM_001201427.2(DAAM2):c.1042A>G (p.Met348Val)	DAAM2 (M348V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2250682	NM_001201427.2(DAAM2):c.1174G>C (p.Gly392Arg)	DAAM2 (G392R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2308068	NM_001201427.2(DAAM2):c.1210A>G (p.Ile404Val)	DAAM2 (I404V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2547832	NM_001201427.2(DAAM2):c.1236T>G (p.Asp412Glu)	DAAM2 (D412E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079853	NM_001201427.2(DAAM2):c.1237G>A (p.Glu413Lys)	DAAM2 (E413K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079854	NM_001201427.2(DAAM2):c.1255G>C (p.Asp419His)	DAAM2 (D419H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2599979	NM_001201427.2(DAAM2):c.1294G>A (p.Val432Ile)	DAAM2 (V432I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2361749	NM_001201427.2(DAAM2):c.1368G>A (p.Met456Ile)	DAAM2 (M456I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3270757	NM_001201427.2(DAAM2):c.1372C>T (p.Leu458Phe)	DAAM2 (L458F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2252411	NM_001201427.2(DAAM2):c.1397A>G (p.Glu466Gly)	DAAM2 (E466G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079856	NM_001201427.2(DAAM2):c.1445C>T (p.Thr482Met)	DAAM2 (T482M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3270758	NM_001201427.2(DAAM2):c.1487A>G (p.Glu496Gly)	DAAM2 (E496G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3270764	NM_001201427.2(DAAM2):c.1497G>C (p.Gln499His)	DAAM2 (Q499H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079857	NM_001201427.2(DAAM2):c.1502G>A (p.Arg501Gln)	DAAM2 (R501Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2407195	NM_001201427.2(DAAM2):c.1559C>T (p.Ser520Phe)	DAAM2 (S520F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2221078	NM_001201427.2(DAAM2):c.1564C>T (p.Pro522Ser)	DAAM2 (P522S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079858	NM_001201427.2(DAAM2):c.1628C>T (p.Pro543Leu)	DAAM2 (P543L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079859	NM_001201427.2(DAAM2):c.1643C>T (p.Pro548Leu)	DAAM2 (P548L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2224436	NM_001201427.2(DAAM2):c.1789C>T (p.Arg597Cys)	DAAM2 (R597C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2399325	NM_001201427.2(DAAM2):c.1790G>C (p.Arg597Pro)	DAAM2 (R597P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2485395	NM_001201427.2(DAAM2):c.1810C>T (p.Pro604Ser)	DAAM2 (P604S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3270756	NM_001201427.2(DAAM2):c.1898G>A (p.Arg633Gln)	DAAM2 (R633Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2241639	NM_001201427.2(DAAM2):c.2026C>T (p.Arg676Trp)	DAAM2 (R676W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2213420	NM_001201427.2(DAAM2):c.2087G>A (p.Arg696Gln)	DAAM2, LOC126859670 (R696Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3046022	NM_001201427.2(DAAM2):c.2095A>G (p.Ile699Val)	DAAM2, LOC126859670 (I699V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2254143	NM_001201427.2(DAAM2):c.2100G>C (p.Leu700Phe)	DAAM2, LOC126859670 (L700F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079861	NM_001201427.2(DAAM2):c.2140G>C (p.Glu714Gln)	DAAM2, LOC126859670 (E714Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2519736	NM_001201427.2(DAAM2):c.2222G>A (p.Arg741His)	DAAM2, DAAM2-AS1 (R741H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2606028	NM_001201427.2(DAAM2):c.2323G>C (p.Ala775Pro)	DAAM2, DAAM2-AS1 (A775P)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2327549	NM_001201427.2(DAAM2):c.2372G>A (p.Arg791His)	DAAM2, DAAM2-AS1 (R791H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2351935	NM_001201427.2(DAAM2):c.2380C>T (p.Arg794Cys)	DAAM2, DAAM2-AS1 (R794C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2554664	NM_001201427.2(DAAM2):c.2446G>A (p.Gly816Ser)	DAAM2, DAAM2-AS1 (G816S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2276348	NM_001201427.2(DAAM2):c.2473C>T (p.Leu825Phe)	DAAM2, DAAM2-AS1 (L825F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2622497	NM_001201427.2(DAAM2):c.2491A>G (p.Thr831Ala)	DAAM2, DAAM2-AS1 (T831A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2320777	NM_001201427.2(DAAM2):c.2512A>C (p.Asn838His)	DAAM2, DAAM2-AS1 (N838H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079862	NM_001201427.2(DAAM2):c.2578C>T (p.Pro860Ser)	DAAM2, DAAM2-AS1 (P860S)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2533016	NM_001201427.2(DAAM2):c.2578C>G (p.Pro860Ala)	DAAM2, DAAM2-AS1 (P860A)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3079863	NM_001201427.2(DAAM2):c.2599C>T (p.Pro867Ser)	DAAM2, DAAM2-AS1 (P867S)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3270760	NM_001201427.2(DAAM2):c.2608G>A (p.Ala870Thr)	DAAM2, DAAM2-AS1 (A870T)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2556342	NM_001201427.2(DAAM2):c.2658G>C (p.Arg886Ser)	DAAM2 (R886S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2207423	NM_001201427.2(DAAM2):c.2677G>C (p.Val893Leu)	DAAM2 (V893L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079864	NM_001201427.2(DAAM2):c.2682G>A (p.Glu894=)	DAAM2	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2256131	NM_001201427.2(DAAM2):c.2698C>T (p.Arg900Cys)	DAAM2 (R899C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2456934	NM_001201427.2(DAAM2):c.2753C>T (p.Thr918Met)	DAAM2 (T917M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2210863	NM_001201427.2(DAAM2):c.2809A>G (p.Lys937Glu)	DAAM2 (K936E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2398386	NM_001201427.2(DAAM2):c.2836G>A (p.Gly946Arg)	DAAM2 (G945R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2298251	NM_001201427.2(DAAM2):c.2842C>A (p.His948Asn)	DAAM2 (H948N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2230233	NM_001201427.2(DAAM2):c.2866G>A (p.Glu956Lys)	DAAM2 (E955K +1 more)	Single nucleotide variant (missense variant)	DAAM2-related disorder +1 more	GUncertain significance
Select item 2475028	NM_001201427.2(DAAM2):c.2876G>C (p.Gly959Ala)	DAAM2 (G958A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079865	NM_001201427.2(DAAM2):c.2884G>C (p.Asp962His)	DAAM2 (D962H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2340664	NM_001201427.2(DAAM2):c.2888C>A (p.Thr963Asn)	DAAM2 (T963N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079866	NM_001201427.2(DAAM2):c.2915G>A (p.Arg972Gln)	DAAM2 (R972Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2291234	NM_001201427.2(DAAM2):c.2942G>A (p.Arg981Lys)	DAAM2 (R980K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2376671	NM_001201427.2(DAAM2):c.2944A>G (p.Lys982Glu)	DAAM2 (K981E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2406650	NM_001201427.2(DAAM2):c.2960G>A (p.Arg987Gln)	DAAM2 (R986Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079867	NM_001201427.2(DAAM2):c.2962C>T (p.Arg988Trp)	DAAM2 (R987W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2401617	NM_001201427.2(DAAM2):c.2966C>T (p.Ala989Val)	DAAM2 (A989V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2364327	NM_001201427.2(DAAM2):c.2969G>A (p.Arg990His)	DAAM2 (R989H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2367225	NM_001201427.2(DAAM2):c.2972T>C (p.Met991Thr)	DAAM2 (M991T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079868	NM_001201427.2(DAAM2):c.3007C>T (p.Arg1003Trp)	DAAM2 (R1002W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2313690	NM_001201427.2(DAAM2):c.3022C>T (p.Arg1008Trp)	DAAM2 (R1008W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2208074	NM_001201427.2(DAAM2):c.3047C>T (p.Ser1016Leu)	DAAM2 (S1015L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455874	NM_001201427.2(DAAM2):c.3092G>A (p.Arg1031His)	DAAM2 (R1030H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3270761	NM_001201427.2(DAAM2):c.3109G>A (p.Asp1037Asn)	DAAM2 (D1036N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2403518	NM_001201427.2(DAAM2):c.3137G>A (p.Ser1046Asn)	DAAM2 (S1046N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455917	NM_001201427.2(DAAM2):c.3139C>T (p.Arg1047Cys)	DAAM2 (R1047C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079869	NM_001201427.2(DAAM2):c.3146G>C (p.Arg1049Pro)	DAAM2 (R1049P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2562189	NM_001201427.2(DAAM2):c.3176G>A (p.Arg1059Gln)	DAAM2 (R1058Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3270759	NM_001201427.2(DAAM2):c.3182G>T (p.Arg1061Leu)	DAAM2 (R1060L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2379205	NM_001201427.2(DAAM2):c.3192C>G (p.Asn1064Lys)	DAAM2 (N1064K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2250389	NM_001201427.2(DAAM2):c.3194G>A (p.Arg1065Gln)	DAAM2 (R1065Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 90