ClinVar for Gene (Select 202333) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3268067	NM_153610.5(CMYA5):c.9238G>A (p.Glu3080Lys)	CMYA5 (E3080K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268066	NM_153610.5(CMYA5):c.1994A>G (p.Gln665Arg)	CMYA5 (Q665R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268065	NM_153610.5(CMYA5):c.6493G>T (p.Asp2165Tyr)	CMYA5 (D2165Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268064	NM_153610.5(CMYA5):c.7108C>G (p.Gln2370Glu)	CMYA5 (Q2370E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268063	NM_153610.5(CMYA5):c.4627G>A (p.Glu1543Lys)	CMYA5 (E1543K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268062	NM_153610.5(CMYA5):c.8342G>C (p.Ser2781Thr)	CMYA5 (S2781T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268061	NM_153610.5(CMYA5):c.9352C>T (p.Pro3118Ser)	CMYA5 (P3118S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268059	NM_153610.5(CMYA5):c.5447A>T (p.Asp1816Val)	CMYA5 (D1816V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268058	NM_153610.5(CMYA5):c.11302T>G (p.Cys3768Gly)	CMYA5 (C3768G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268057	NM_153610.5(CMYA5):c.8190T>G (p.Cys2730Trp)	CMYA5 (C2730W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268056	NM_153610.5(CMYA5):c.11174T>C (p.Val3725Ala)	CMYA5 (V3725A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268055	NM_153610.5(CMYA5):c.8657C>T (p.Ser2886Phe)	CMYA5 (S2886F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268054	NM_153610.5(CMYA5):c.5572A>G (p.Arg1858Gly)	CMYA5 (R1858G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268053	NM_153610.5(CMYA5):c.484C>T (p.Pro162Ser)	CMYA5 (P162S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268052	NM_153610.5(CMYA5):c.11035C>A (p.Pro3679Thr)	CMYA5 (P3679T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268051	NM_153610.5(CMYA5):c.4767T>G (p.Asp1589Glu)	CMYA5 (D1589E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268050	NM_153610.5(CMYA5):c.9569C>G (p.Ala3190Gly)	CMYA5 (A3190G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268048	NM_153610.5(CMYA5):c.11395A>G (p.Ile3799Val)	CMYA5 (I3799V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268047	NM_153610.5(CMYA5):c.9355G>A (p.Glu3119Lys)	CMYA5 (E3119K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268046	NM_153610.5(CMYA5):c.6376G>A (p.Val2126Ile)	CMYA5 (V2126I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268045	NM_153610.5(CMYA5):c.1208C>T (p.Pro403Leu)	CMYA5 (P403L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268044	NM_153610.5(CMYA5):c.670A>C (p.Thr224Pro)	CMYA5 (T224P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268043	NM_153610.5(CMYA5):c.2114T>G (p.Leu705Arg)	CMYA5 (L705R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268042	NM_153610.5(CMYA5):c.6518A>C (p.Lys2173Thr)	CMYA5 (K2173T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268041	NM_153610.5(CMYA5):c.10175A>G (p.Gln3392Arg)	CMYA5 (Q3392R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268040	NM_153610.5(CMYA5):c.4864C>A (p.Pro1622Thr)	CMYA5 (P1622T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268039	NM_153610.5(CMYA5):c.8005C>G (p.His2669Asp)	CMYA5 (H2669D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268037	NM_153610.5(CMYA5):c.10420A>G (p.Thr3474Ala)	CMYA5 (T3474A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268036	NM_153610.5(CMYA5):c.5453T>C (p.Leu1818Pro)	CMYA5 (L1818P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268035	NM_153610.5(CMYA5):c.830G>A (p.Gly277Asp)	CMYA5 (G277D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3268034	NM_153610.5(CMYA5):c.6914C>T (p.Ser2305Leu)	CMYA5 (S2305L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268033	NM_153610.5(CMYA5):c.1090C>T (p.Pro364Ser)	CMYA5 (P364S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268032	NM_153610.5(CMYA5):c.10756A>G (p.Lys3586Glu)	CMYA5 (K3586E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268031	NM_153610.5(CMYA5):c.100G>A (p.Gly34Ser)	CMYA5 (G34S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268030	NM_153610.5(CMYA5):c.701C>T (p.Ser234Leu)	CMYA5 (S234L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268029	NM_153610.5(CMYA5):c.2716C>T (p.Pro906Ser)	CMYA5 (P906S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268026	NM_153610.5(CMYA5):c.11476C>T (p.Arg3826Trp)	CMYA5 (R3826W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268025	NM_153610.5(CMYA5):c.9416A>G (p.Asn3139Ser)	CMYA5 (N3139S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268024	NM_153610.5(CMYA5):c.11000C>T (p.Ser3667Phe)	CMYA5 (S3667F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268023	NM_153610.5(CMYA5):c.10478C>T (p.Ser3493Phe)	CMYA5 (S3493F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268022	NM_153610.5(CMYA5):c.533C>T (p.Thr178Ile)	CMYA5 (T178I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268021	NM_153610.5(CMYA5):c.9962A>G (p.Lys3321Arg)	CMYA5 (K3321R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3268020	NM_153610.5(CMYA5):c.6275G>T (p.Ser2092Ile)	CMYA5 (S2092I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268019	NM_153610.5(CMYA5):c.10767A>T (p.Glu3589Asp)	CMYA5 (E3589D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268018	NM_153610.5(CMYA5):c.12064T>C (p.Phe4022Leu)	CMYA5 (F4022L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146377	NM_153610.5(CMYA5):c.9949G>A (p.Val3317Ile)	CMYA5 (V3317I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3146376	NM_153610.5(CMYA5):c.9817T>C (p.Tyr3273His)	CMYA5 (Y3273H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146375	NM_153610.5(CMYA5):c.9811G>A (p.Asp3271Asn)	CMYA5 (D3271N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146374	NM_153610.5(CMYA5):c.9772C>G (p.Gln3258Glu)	CMYA5 (Q3258E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146373	NM_153610.5(CMYA5):c.9458C>A (p.Pro3153Gln)	CMYA5 (P3153Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146372	NM_153610.5(CMYA5):c.9434A>G (p.Lys3145Arg)	CMYA5 (K3145R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146371	NM_153610.5(CMYA5):c.9304C>G (p.Leu3102Val)	CMYA5 (L3102V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146370	NM_153610.5(CMYA5):c.9136A>G (p.Ile3046Val)	CMYA5 (I3046V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146367	NM_153610.5(CMYA5):c.8962A>C (p.Thr2988Pro)	CMYA5 (T2988P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146366	NM_153610.5(CMYA5):c.8771G>A (p.Gly2924Asp)	CMYA5 (G2924D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3146365	NM_153610.5(CMYA5):c.8756A>G (p.Asp2919Gly)	CMYA5 (D2919G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146364	NM_153610.5(CMYA5):c.8627C>A (p.Ala2876Glu)	CMYA5 (A2876E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146363	NM_153610.5(CMYA5):c.8458C>T (p.Leu2820Phe)	CMYA5 (L2820F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146362	NM_153610.5(CMYA5):c.8422C>G (p.Pro2808Ala)	CMYA5 (P2808A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146360	NM_153610.5(CMYA5):c.8268T>A (p.Asp2756Glu)	CMYA5 (D2756E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146359	NM_153610.5(CMYA5):c.8110G>A (p.Gly2704Arg)	CMYA5 (G2704R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146358	NM_153610.5(CMYA5):c.7928G>T (p.Arg2643Leu)	CMYA5 (R2643L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146357	NM_153610.5(CMYA5):c.7735T>G (p.Ser2579Ala)	CMYA5 (S2579A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146356	NM_153610.5(CMYA5):c.7662G>T (p.Gln2554His)	CMYA5 (Q2554H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146355	NM_153610.5(CMYA5):c.7531G>A (p.Asp2511Asn)	CMYA5 (D2511N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3146354	NM_153610.5(CMYA5):c.7462A>G (p.Ser2488Gly)	CMYA5 (S2488G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146353	NM_153610.5(CMYA5):c.7351G>A (p.Val2451Ile)	CMYA5 (V2451I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146352	NM_153610.5(CMYA5):c.7309A>G (p.Thr2437Ala)	CMYA5 (T2437A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146351	NM_153610.5(CMYA5):c.6758T>C (p.Leu2253Ser)	CMYA5 (L2253S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146350	NM_153610.5(CMYA5):c.6728T>G (p.Leu2243Arg)	CMYA5 (L2243R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146349	NM_153610.5(CMYA5):c.6649A>G (p.Ile2217Val)	CMYA5 (I2217V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146348	NM_153610.5(CMYA5):c.6530C>A (p.Ser2177Tyr)	CMYA5 (S2177Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146347	NM_153610.5(CMYA5):c.6391C>G (p.Gln2131Glu)	CMYA5 (Q2131E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146346	NM_153610.5(CMYA5):c.6322G>A (p.Val2108Ile)	CMYA5 (V2108I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146345	NM_153610.5(CMYA5):c.590C>G (p.Thr197Ser)	CMYA5 (T197S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146344	NM_153610.5(CMYA5):c.5860T>A (p.Ser1954Thr)	CMYA5 (S1954T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146343	NM_153610.5(CMYA5):c.5367G>C (p.Lys1789Asn)	CMYA5 (K1789N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146342	NM_153610.5(CMYA5):c.5365A>G (p.Lys1789Glu)	CMYA5 (K1789E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146341	NM_153610.5(CMYA5):c.522C>G (p.Ser174Arg)	CMYA5 (S174R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146340	NM_153610.5(CMYA5):c.4981A>G (p.Ile1661Val)	CMYA5 (I1661V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146339	NM_153610.5(CMYA5):c.4904C>T (p.Pro1635Leu)	CMYA5 (P1635L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146338	NM_153610.5(CMYA5):c.4837G>A (p.Val1613Ile)	CMYA5 (V1613I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3146337	NM_153610.5(CMYA5):c.4661C>T (p.Ser1554Phe)	CMYA5 (S1554F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146336	NM_153610.5(CMYA5):c.449A>G (p.Asn150Ser)	CMYA5 (N150S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146335	NM_153610.5(CMYA5):c.4282G>A (p.Glu1428Lys)	CMYA5 (E1428K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146334	NM_153610.5(CMYA5):c.3961T>C (p.Ser1321Pro)	CMYA5 (S1321P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3146332	NM_153610.5(CMYA5):c.3841C>T (p.Pro1281Ser)	CMYA5 (P1281S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146331	NM_153610.5(CMYA5):c.3740T>C (p.Val1247Ala)	CMYA5 (V1247A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146330	NM_153610.5(CMYA5):c.3634G>C (p.Asp1212His)	CMYA5 (D1212H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146329	NM_153610.5(CMYA5):c.3556C>A (p.Pro1186Thr)	CMYA5 (P1186T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146328	NM_153610.5(CMYA5):c.3524A>G (p.Asp1175Gly)	CMYA5 (D1175G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146327	NM_153610.5(CMYA5):c.3493A>G (p.Lys1165Glu)	CMYA5 (K1165E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146326	NM_153610.5(CMYA5):c.325C>T (p.Arg109Trp)	CMYA5 (R109W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146325	NM_153610.5(CMYA5):c.3202A>G (p.Thr1068Ala)	CMYA5 (T1068A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146324	NM_153610.5(CMYA5):c.3047C>T (p.Thr1016Ile)	CMYA5 (T1016I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146323	NM_153610.5(CMYA5):c.2675G>A (p.Arg892Gln)	CMYA5 (R892Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146321	NM_153610.5(CMYA5):c.2635T>C (p.Tyr879His)	CMYA5 (Y879H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3146320	NM_153610.5(CMYA5):c.2298G>C (p.Gln766His)	CMYA5 (Q766H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146319	NM_153610.5(CMYA5):c.2252A>G (p.Glu751Gly)	CMYA5 (E751G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3146318	NM_153610.5(CMYA5):c.1952G>A (p.Ser651Asn)	CMYA5 (S651N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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