Related gene-specific medical variations for Gene (Select 100527960) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3206438	NM_001039464.4(MROH7):c.899T>A (p.Leu300Gln)	MROH7, MROH7-TTC4 (L300Q)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206434	NM_001039464.4(MROH7):c.880C>G (p.Gln294Glu)	MROH7, MROH7-TTC4 (Q294E)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206427	NM_001039464.4(MROH7):c.712G>A (p.Gly238Arg)	MROH7, MROH7-TTC4 (G238R)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206423	NM_001039464.4(MROH7):c.692A>G (p.Asn231Ser)	MROH7, MROH7-TTC4 (N231S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206399	NM_001039464.4(MROH7):c.3791A>G (p.Gln1264Arg)	MROH7, MROH7-TTC4 (Q1264R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3206396	NM_001039464.4(MROH7):c.3727G>A (p.Ala1243Thr)	MROH7, MROH7-TTC4 (A761T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206392	NM_001039464.4(MROH7):c.3665T>C (p.Ile1222Thr)	MROH7, MROH7-TTC4 (I1222T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206373	NM_001039464.4(MROH7):c.359G>A (p.Arg120His)	MROH7, MROH7-TTC4 (R120H)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign
Select item 3206359	NM_001039464.4(MROH7):c.356G>C (p.Gly119Ala)	MROH7, MROH7-TTC4 (G119A)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206353	NM_001039464.4(MROH7):c.34C>G (p.His12Asp)	MROH7, MROH7-TTC4 (H12D)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206349	NM_001039464.4(MROH7):c.3355C>T (p.Arg1119Cys)	MROH7, MROH7-TTC4 (R637C +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3206301	NM_001039464.4(MROH7):c.2921G>A (p.Gly974Asp)	MROH7, MROH7-TTC4 (G492D +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206297	NM_001039464.4(MROH7):c.2885G>A (p.Arg962His)	MROH7, MROH7-TTC4 (R480H +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206287	NM_001039464.4(MROH7):c.2782G>A (p.Asp928Asn)	MROH7, MROH7-TTC4 (D446N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206280	NM_001039464.4(MROH7):c.272C>T (p.Pro91Leu)	MROH7, MROH7-TTC4 (P91L)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206271	NM_001039464.4(MROH7):c.2570G>T (p.Arg857Leu)	MROH7, MROH7-TTC4 (R857L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206256	NM_001039464.4(MROH7):c.2450A>C (p.Asp817Ala)	MROH7, MROH7-TTC4 (D335A +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206246	NM_001039464.4(MROH7):c.2311T>A (p.Ser771Thr)	MROH7, MROH7-TTC4 (S289T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206241	NM_001039464.4(MROH7):c.22A>G (p.Asn8Asp)	MROH7, MROH7-TTC4 (N8D)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206237	NM_001039464.4(MROH7):c.2281C>T (p.Arg761Trp)	MROH7, MROH7-TTC4 (R279W +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206214	NM_001039464.4(MROH7):c.2087A>G (p.Asp696Gly)	MROH7, MROH7-TTC4 (D214G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206206	NM_001039464.4(MROH7):c.1803G>T (p.Met601Ile)	MROH7, MROH7-TTC4 (M601I +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206187	NM_001039464.4(MROH7):c.1572G>T (p.Lys524Asn)	MROH7, MROH7-TTC4 (K42N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3206179	NM_001039464.4(MROH7):c.1454T>C (p.Ile485Thr)	MROH7, MROH7-TTC4 (I485T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3206178	NM_001039464.4(MROH7):c.1430C>A (p.Ser477Tyr)	MROH7, MROH7-TTC4 (S477Y)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206176	NM_001039464.4(MROH7):c.1382A>G (p.Lys461Arg)	MROH7, MROH7-TTC4 (K461R)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206172	NM_001039464.4(MROH7):c.1304T>C (p.Leu435Pro)	MROH7, MROH7-TTC4 (L435P)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206167	NM_001039464.4(MROH7):c.1242T>A (p.Asp414Glu)	MROH7, MROH7-TTC4 (D414E)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3206157	NM_001039464.4(MROH7):c.1018G>A (p.Asp340Asn)	MROH7, MROH7-TTC4 (D340N)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3184369	NM_004623.5(TTC4):c.817A>G (p.Arg273Gly)	MROH7-TTC4, TTC4 (R273G)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3184368	NM_004623.5(TTC4):c.786T>A (p.His262Gln)	MROH7-TTC4, TTC4 (H262Q)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3184367	NM_004623.5(TTC4):c.377C>T (p.Ala126Val)	MROH7-TTC4, TTC4 (A126V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3184366	NM_004623.5(TTC4):c.335A>G (p.Asp112Gly)	MROH7-TTC4, TTC4 (D112G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3184365	NM_004623.5(TTC4):c.233A>G (p.Gln78Arg)	MROH7-TTC4, TTC4 (Q78R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3184364	NM_004623.5(TTC4):c.1102G>A (p.Val368Ile)	MROH7-TTC4, TTC4 (V368I +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3025056	NM_001039464.4(MROH7):c.1188C>A (p.Asn396Lys)	MROH7, MROH7-TTC4 (N396K)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2638835	NM_001039464.4(MROH7):c.3729T>A (p.Ala1243=)	MROH7, MROH7-TTC4	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2638834	NM_001039464.4(MROH7):c.3286-4C>T	MROH7, MROH7-TTC4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2638833	NM_001039464.4(MROH7):c.1203C>T (p.Asp401=)	MROH7, MROH7-TTC4	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2638832	NM_001039464.4(MROH7):c.1191C>T (p.Pro397=)	MROH7, MROH7-TTC4	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2638831	NM_001039464.4(MROH7):c.594A>G (p.Ser198=)	MROH7, MROH7-TTC4	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2638830	NM_001039464.4(MROH7):c.191C>G (p.Ser64Cys)	MROH7, MROH7-TTC4 (S64C)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2621066	NM_001039464.4(MROH7):c.3149T>C (p.Leu1050Pro)	MROH7, MROH7-TTC4 (L1050P +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2619555	NM_004623.5(TTC4):c.103T>C (p.Trp35Arg)	MROH7-TTC4, TTC4 (W35R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611115	NM_001039464.4(MROH7):c.2099C>A (p.Ala700Asp)	MROH7, MROH7-TTC4 (A218D +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2594913	NM_001039464.4(MROH7):c.3920G>A (p.Arg1307His)	MROH7, MROH7-TTC4 (R1307H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590222	NM_001039464.4(MROH7):c.3578G>A (p.Arg1193Gln)	MROH7, MROH7-TTC4 (R1193Q +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2568682	NM_001039464.4(MROH7):c.1817C>T (p.Pro606Leu)	MROH7, MROH7-TTC4 (P606L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2558847	NM_001039464.4(MROH7):c.3631C>T (p.Arg1211Trp)	MROH7, MROH7-TTC4 (R1211W +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2551355	NM_001039464.4(MROH7):c.2189C>T (p.Ser730Leu)	MROH7, MROH7-TTC4 (S730L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2543303	NM_004623.5(TTC4):c.979G>C (p.Val327Leu)	MROH7-TTC4, TTC4 (V228L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2542980	NM_004623.5(TTC4):c.779A>T (p.Asn260Ile)	MROH7-TTC4, TTC4 (N260I)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2526267	NM_004623.5(TTC4):c.686G>C (p.Arg229Thr)	MROH7-TTC4, TTC4 (R229T)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2522840	NM_001039464.4(MROH7):c.3215G>A (p.Arg1072Gln)	MROH7, MROH7-TTC4 (R590Q +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2515099	NM_001039464.4(MROH7):c.3601A>G (p.Ser1201Gly)	MROH7, MROH7-TTC4 (S1201G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2507692	NM_001039464.4(MROH7):c.2171C>T (p.Ser724Leu)	MROH7, MROH7-TTC4 (S724L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2492607	NM_001039464.4(MROH7):c.1580C>T (p.Ala527Val)	MROH7, MROH7-TTC4 (A527V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2489725	NM_001039464.4(MROH7):c.3315C>G (p.Ile1105Met)	MROH7, MROH7-TTC4 (I623M +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2485133	NM_001039464.4(MROH7):c.2177T>C (p.Val726Ala)	MROH7, MROH7-TTC4 (V244A +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2484062	NM_001039464.4(MROH7):c.3029G>T (p.Gly1010Val)	MROH7, MROH7-TTC4 (G528V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2460783	NM_004623.5(TTC4):c.863C>T (p.Ser288Leu)	MROH7-TTC4, TTC4 (S288L)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2457848	NM_001039464.4(MROH7):c.3071G>A (p.Arg1024Gln)	MROH7, MROH7-TTC4 (R1024Q +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2455876	NM_001039464.4(MROH7):c.2884C>T (p.Arg962Cys)	MROH7, MROH7-TTC4 (R480C +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2454820	NM_001039464.4(MROH7):c.953A>G (p.Asn318Ser)	MROH7, MROH7-TTC4 (N318S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2408220	NM_001039464.4(MROH7):c.3182C>T (p.Ala1061Val)	MROH7, MROH7-TTC4 (A1061V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2405692	NM_001039464.4(MROH7):c.1655T>A (p.Ile552Asn)	MROH7-TTC4, MROH7 (I552N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2401584	NM_001039464.4(MROH7):c.358C>T (p.Arg120Cys)	MROH7, MROH7-TTC4 (R120C)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2400140	NM_001039464.4(MROH7):c.3272C>T (p.Pro1091Leu)	MROH7, MROH7-TTC4 (P1091L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2397007	NM_001039464.4(MROH7):c.719T>G (p.Leu240Arg)	MROH7, MROH7-TTC4 (L240R)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2396222	NM_001039464.4(MROH7):c.316G>T (p.Asp106Tyr)	MROH7, MROH7-TTC4 (D106Y)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2388672	NM_001039464.4(MROH7):c.1981A>G (p.Ser661Gly)	MROH7, MROH7-TTC4 (S179G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2376240	NM_001039464.4(MROH7):c.3016C>T (p.Arg1006Trp)	MROH7, MROH7-TTC4 (R1006W +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2374229	NM_001039464.4(MROH7):c.3091C>G (p.Arg1031Gly)	MROH7, MROH7-TTC4 (R1031G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2373289	NM_001039464.4(MROH7):c.3947C>T (p.Ser1316Phe)	MROH7, MROH7-TTC4 (S1316F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372325	NM_001039464.4(MROH7):c.3305C>T (p.Ser1102Phe)	MROH7, MROH7-TTC4 (S1102F +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2366303	NM_001039464.4(MROH7):c.2102C>T (p.Ala701Val)	MROH7, MROH7-TTC4 (A701V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2362290	NM_001039464.4(MROH7):c.233A>G (p.Glu78Gly)	MROH7, MROH7-TTC4 (E78G)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2358124	NM_001039464.4(MROH7):c.1736G>A (p.Arg579Gln)	MROH7, MROH7-TTC4 (R579Q +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2343355	NM_001039464.4(MROH7):c.1096C>T (p.His366Tyr)	MROH7, MROH7-TTC4 (H366Y)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2341829	NM_001039464.4(MROH7):c.2101G>A (p.Ala701Thr)	MROH7, MROH7-TTC4 (A701T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2335601	NM_001039464.4(MROH7):c.1235C>T (p.Ala412Val)	MROH7, MROH7-TTC4 (A412V)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2332353	NM_001039464.4(MROH7):c.3218A>G (p.Asp1073Gly)	MROH7, MROH7-TTC4 (D591G +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2331153	NM_001039464.4(MROH7):c.2287C>T (p.Arg763Cys)	MROH7, MROH7-TTC4 (R281C +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2325874	NM_001039464.4(MROH7):c.1558G>A (p.Ala520Thr)	MROH7, MROH7-TTC4 (A520T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2324354	NM_001039464.4(MROH7):c.407C>T (p.Ala136Val)	MROH7, MROH7-TTC4 (A136V)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2320091	NM_001039464.4(MROH7):c.1006A>T (p.Thr336Ser)	MROH7, MROH7-TTC4 (T336S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2318456	NM_001039464.4(MROH7):c.2444T>G (p.Leu815Arg)	MROH7, MROH7-TTC4 (L815R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2311855	NM_001039464.4(MROH7):c.2512C>A (p.Pro838Thr)	MROH7, MROH7-TTC4 (P356T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2310811	NM_001039464.4(MROH7):c.2710C>T (p.Arg904Cys)	MROH7, MROH7-TTC4 (R422C +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2301190	NM_001039464.4(MROH7):c.3592A>C (p.Ile1198Leu)	MROH7, MROH7-TTC4 (I1198L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2298122	NM_001039464.4(MROH7):c.3821A>G (p.Asn1274Ser)	MROH7, MROH7-TTC4 (N1274S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296736	NM_004623.5(TTC4):c.88T>A (p.Phe30Ile)	MROH7-TTC4, TTC4 (F30I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285989	NM_004623.5(TTC4):c.19G>A (p.Asp7Asn)	MROH7-TTC4, TTC4 (D7N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283073	NM_001039464.4(MROH7):c.3877T>A (p.Trp1293Arg)	MROH7, MROH7-TTC4 (W811R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2280182	NM_001039464.4(MROH7):c.166G>C (p.Ala56Pro)	MROH7, MROH7-TTC4 (A56P)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2280067	NM_001039464.4(MROH7):c.668G>T (p.Arg223Ile)	MROH7, MROH7-TTC4 (R223I)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2254226	NM_004623.5(TTC4):c.683C>T (p.Ala228Val)	MROH7-TTC4, TTC4 (A228V)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2241352	NM_001039464.4(MROH7):c.1379A>G (p.Lys460Arg)	MROH7, MROH7-TTC4 (K460R)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2236115	NM_001039464.4(MROH7):c.2570G>A (p.Arg857His)	MROH7, MROH7-TTC4 (R375H +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2230540	NM_001039464.4(MROH7):c.3210G>T (p.Lys1070Asn)	MROH7, MROH7-TTC4 (K1070N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

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