FGD6[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 77

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2290096	NM_018351.4(FGD6):c.4111G>A (p.Val1371Met)	FGD6 (V1371M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094686	NM_018351.4(FGD6):c.4033G>A (p.Gly1345Ser)	FGD6 (G1345S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094685	NM_018351.4(FGD6):c.3459G>C (p.Lys1153Asn)	FGD6 (K1153N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094684	NM_018351.4(FGD6):c.3320G>C (p.Arg1107Pro)	FGD6 (R1107P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094682	NM_018351.4(FGD6):c.3196A>G (p.Asn1066Asp)	FGD6 (N1066D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483711	NM_018351.4(FGD6):c.2923A>G (p.Lys975Glu)	FGD6 (K975E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781089	NM_018351.4(FGD6):c.2837+8T>G	FGD6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2322042	NM_018351.4(FGD6):c.2797C>T (p.Arg933Trp)	FGD6 (R933W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273749	NM_018351.4(FGD6):c.2786A>G (p.Tyr929Cys)	FGD6 (Y929C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094677	NM_018351.4(FGD6):c.2746C>T (p.Arg916Trp)	FGD6 (R916W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 784253	NM_018351.4(FGD6):c.2655-4A>T	FGD6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3094676	NM_018351.4(FGD6):c.2617C>T (p.His873Tyr)	FGD6 (H873Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218632	NM_018351.4(FGD6):c.2603T>G (p.Met868Arg)	FGD6 (M868R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608336	NM_018351.4(FGD6):c.2560G>A (p.Glu854Lys)	FGD6 (E854K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094675	NM_018351.4(FGD6):c.2487C>A (p.Asp829Glu)	FGD6 (D829E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2408797	NM_018351.4(FGD6):c.2444C>T (p.Ser815Leu)	FGD6 (S815L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515883	NM_018351.4(FGD6):c.2257C>T (p.His753Tyr)	FGD6 (H753Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094673	NM_018351.4(FGD6):c.2254C>T (p.Arg752Cys)	FGD6 (R752C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469982	NM_018351.4(FGD6):c.2237C>T (p.Pro746Leu)	FGD6 (P746L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094672	NM_018351.4(FGD6):c.2231G>C (p.Cys744Ser)	FGD6 (C744S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237621	NM_018351.4(FGD6):c.2144A>G (p.Asn715Ser)	FGD6 (N715S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343329	NM_018351.4(FGD6):c.2122C>T (p.Arg708Trp)	FGD6 (R708W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094671	NM_018351.4(FGD6):c.2054G>T (p.Ser685Ile)	FGD6 (S685I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277207	NM_018351.4(FGD6):c.2035G>T (p.Val679Leu)	FGD6 (V679L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094670	NM_018351.4(FGD6):c.1963G>A (p.Gly655Arg)	FGD6 (G655R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094669	NM_018351.4(FGD6):c.1918A>T (p.Met640Leu)	FGD6 (M640L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411470	NM_018351.4(FGD6):c.1894A>G (p.Ser632Gly)	FGD6 (S632G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278614	NM_018351.4(FGD6):c.1850C>T (p.Pro617Leu)	FGD6 (P617L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094668	NM_018351.4(FGD6):c.1837A>C (p.Lys613Gln)	FGD6 (K613Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205544	NM_018351.4(FGD6):c.1651G>A (p.Val551Met)	FGD6 (V551M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2281878	NM_018351.4(FGD6):c.1642A>C (p.Asn548His)	FGD6 (N548H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281877	NM_018351.4(FGD6):c.1641A>C (p.Gln547His)	FGD6 (Q547H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285190	NM_018351.4(FGD6):c.1640A>C (p.Gln547Pro)	FGD6 (Q547P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2539506	NM_018351.4(FGD6):c.1633T>C (p.Cys545Arg)	FGD6 (C545R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094667	NM_018351.4(FGD6):c.1605T>A (p.Ser535Arg)	FGD6 (S535R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094666	NM_018351.4(FGD6):c.1579A>C (p.Ser527Arg)	FGD6 (S527R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094665	NM_018351.4(FGD6):c.1546G>A (p.Glu516Lys)	FGD6 (E516K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460861	NM_018351.4(FGD6):c.1489A>C (p.Lys497Gln)	FGD6 (K497Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354573	NM_018351.4(FGD6):c.1333G>A (p.Gly445Ser)	FGD6 (G445S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2406462	NM_018351.4(FGD6):c.1259A>T (p.Lys420Ile)	FGD6 (K420I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394723	NM_018351.4(FGD6):c.1255G>A (p.Asp419Asn)	FGD6 (D419N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094664	NM_018351.4(FGD6):c.1211T>C (p.Met404Thr)	FGD6 (M404T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781817	NM_018351.4(FGD6):c.1208C>T (p.Ala403Val)	FGD6 (A403V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2234131	NM_018351.4(FGD6):c.1207G>A (p.Ala403Thr)	FGD6 (A403T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339626	NM_018351.4(FGD6):c.1112A>G (p.Lys371Arg)	FGD6 (K371R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282042	NM_018351.4(FGD6):c.1097A>G (p.Gln366Arg)	FGD6 (Q366R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094662	NM_018351.4(FGD6):c.1084A>G (p.Ser362Gly)	FGD6 (S362G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094661	NM_018351.4(FGD6):c.1065T>A (p.Ser355Arg)	FGD6 (S355R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463171	NM_018351.4(FGD6):c.1022C>T (p.Pro341Leu)	FGD6 (P341L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522090	NM_018351.4(FGD6):c.1008A>C (p.Glu336Asp)	FGD6 (E336D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364562	NM_018351.4(FGD6):c.971G>A (p.Arg324His)	FGD6 (R324H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278613	NM_018351.4(FGD6):c.941C>T (p.Thr314Ile)	FGD6 (T314I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278616	NM_018351.4(FGD6):c.835A>G (p.Lys279Glu)	FGD6 (K279E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237551	NM_018351.4(FGD6):c.827A>G (p.Glu276Gly)	FGD6 (E276G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094689	NM_018351.4(FGD6):c.790A>G (p.Asn264Asp)	FGD6 (N264D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600443	NM_018351.4(FGD6):c.788G>A (p.Ser263Asn)	FGD6 (S263N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568639	NM_018351.4(FGD6):c.739A>G (p.Ser247Gly)	FGD6 (S247G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 728883	NM_018351.4(FGD6):c.683C>A (p.Ser228Tyr)	FGD6 (S228Y)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2246234	NM_018351.4(FGD6):c.616C>T (p.Pro206Ser)	FGD6 (P206S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094688	NM_018351.4(FGD6):c.614G>A (p.Ser205Asn)	FGD6 (S205N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2246716	NM_018351.4(FGD6):c.583A>G (p.Ile195Val)	FGD6 (I195V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609018	NM_018351.4(FGD6):c.573G>A (p.Met191Ile)	FGD6 (M191I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514051	NM_018351.4(FGD6):c.550A>C (p.Lys184Gln)	FGD6 (K184Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528841	NM_018351.4(FGD6):c.540A>C (p.Glu180Asp)	FGD6 (E180D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094687	NM_018351.4(FGD6):c.532G>A (p.Val178Ile)	FGD6 (V178I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3278615	NM_018351.4(FGD6):c.520T>G (p.Leu174Val)	FGD6 (L174V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278612	NM_018351.4(FGD6):c.487G>A (p.Gly163Ser)	FGD6 (G163S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094683	NM_018351.4(FGD6):c.325A>G (p.Met109Val)	FGD6 (M109V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3094681	NM_018351.4(FGD6):c.314A>G (p.Tyr105Cys)	FGD6 (Y105C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094679	NM_018351.4(FGD6):c.301C>A (p.Gln101Lys)	FGD6 (Q101K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094678	NM_018351.4(FGD6):c.298A>C (p.Asn100His)	FGD6 (N100H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3094674	NM_018351.4(FGD6):c.230T>C (p.Leu77Ser)	FGD6 (L77S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613296	NM_018351.4(FGD6):c.152C>T (p.Ala51Val)	FGD6 (A51V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094691	NM_018351.4(FGD6):c.88A>G (p.Ile30Val)	FGD6 (I30V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2350296	NM_018351.4(FGD6):c.56T>C (p.Val19Ala)	FGD6 (V19A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365994	NM_018351.4(FGD6):c.37G>A (p.Ala13Thr)	FGD6 (A13T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1340322	GRCh37/hg19 12q22(chr12:95475366-95601325)x1	FGD6	Copy number loss	not provided	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 77