"Ambry Genetics"[submitter] AND "FLG"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3095429	NM_002016.2(FLG):c.12170A>G (p.Tyr4057Cys)	CCDST, FLG (Y4057C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2602591	NM_002016.2(FLG):c.12128G>A (p.Ser4043Asn)	CCDST, FLG (S4043N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095427	NM_002016.2(FLG):c.12089C>G (p.Thr4030Arg)	CCDST, FLG (T4030R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2527343	NM_002016.2(FLG):c.12068A>T (p.Asp4023Val)	CCDST, FLG (D4023V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095426	NM_002016.2(FLG):c.12004A>G (p.Asn4002Asp)	CCDST, FLG (N4002D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095425	NM_002016.2(FLG):c.11996T>C (p.Val3999Ala)	CCDST, FLG (V3999A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2342265	NM_002016.2(FLG):c.11989G>C (p.Gly3997Arg)	CCDST, FLG (G3997R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2358391	NM_002016.2(FLG):c.11941A>G (p.Ser3981Gly)	CCDST, FLG (S3981G)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3279077	NM_002016.2(FLG):c.11872T>A (p.Tyr3958Asn)	CCDST, FLG (Y3958N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2253092	NM_002016.2(FLG):c.11839C>A (p.Arg3947Ser)	CCDST, FLG (R3947S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2519064	NM_002016.2(FLG):c.11827G>A (p.Gly3943Arg)	CCDST, FLG (G3943R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095424	NM_002016.2(FLG):c.11783A>C (p.His3928Pro)	CCDST, FLG (H3928P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279086	NM_002016.2(FLG):c.11741A>T (p.Gln3914Leu)	CCDST, FLG (Q3914L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2223168	NM_002016.2(FLG):c.11723A>G (p.Asp3908Gly)	CCDST, FLG (D3908G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2570515	NM_002016.2(FLG):c.11720G>A (p.Arg3907His)	CCDST, FLG (R3907H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2325637	NM_002016.2(FLG):c.11714C>T (p.Ser3905Phe)	CCDST, FLG (S3905F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279084	NM_002016.2(FLG):c.11671T>G (p.Ser3891Ala)	CCDST, FLG (S3891A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095423	NM_002016.2(FLG):c.11661T>G (p.His3887Gln)	CCDST, FLG (H3887Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2254158	NM_002016.2(FLG):c.11636G>A (p.Arg3879Gln)	CCDST, FLG (R3879Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3095422	NM_002016.2(FLG):c.11622G>C (p.Glu3874Asp)	CCDST, FLG (E3874D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095421	NM_002016.2(FLG):c.11611G>A (p.Ala3871Thr)	CCDST, FLG (A3871T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2358903	NM_002016.2(FLG):c.11567G>A (p.Ser3856Asn)	CCDST, FLG (S3856N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279119	NM_002016.2(FLG):c.11560A>G (p.Arg3854Gly)	CCDST, FLG (R3854G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279075	NM_002016.2(FLG):c.11555G>A (p.Gly3852Glu)	CCDST, FLG (G3852E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2570519	NM_002016.2(FLG):c.11554G>A (p.Gly3852Arg)	CCDST, FLG (G3852R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593750	NM_002016.2(FLG):c.11537G>A (p.Gly3846Asp)	CCDST, FLG (G3846D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345496	NM_002016.2(FLG):c.11440C>T (p.Arg3814Cys)	CCDST, FLG (R3814C)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3095420	NM_002016.2(FLG):c.11402A>T (p.His3801Leu)	CCDST, FLG (H3801L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2341645	NM_002016.2(FLG):c.11402A>C (p.His3801Pro)	CCDST, FLG (H3801P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095419	NM_002016.2(FLG):c.11380C>A (p.Gln3794Lys)	CCDST, FLG (Q3794K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2393729	NM_002016.2(FLG):c.11317T>C (p.Tyr3773His)	CCDST, FLG (Y3773H)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3025045	NM_002016.2(FLG):c.11312G>T (p.Gly3771Val)	CCDST, FLG (G3771V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2393728	NM_002016.2(FLG):c.11299G>A (p.Gly3767Arg)	CCDST, FLG (G3767R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095418	NM_002016.2(FLG):c.11266G>A (p.Asp3756Asn)	CCDST, FLG (D3756N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2393705	NM_002016.2(FLG):c.11259G>T (p.Glu3753Asp)	CCDST, FLG (E3753D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471903	NM_002016.2(FLG):c.11249C>T (p.Ala3750Val)	CCDST, FLG (A3750V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2294794	NM_002016.2(FLG):c.11248G>A (p.Ala3750Thr)	CCDST, FLG (A3750T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095417	NM_002016.2(FLG):c.11235C>A (p.Ser3745Arg)	CCDST, FLG (S3745R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095416	NM_002016.2(FLG):c.11217C>G (p.His3739Gln)	CCDST, FLG (H3739Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2568730	NM_002016.2(FLG):c.11212C>T (p.Arg3738Cys)	CCDST, FLG (R3738C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095415	NM_002016.2(FLG):c.11207G>T (p.Gly3736Val)	CCDST, FLG (G3736V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2406856	NM_002016.2(FLG):c.11198G>T (p.Gly3733Val)	CCDST, FLG (G3733V)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2393727	NM_002016.2(FLG):c.11197G>C (p.Gly3733Arg)	CCDST, FLG (G3733R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2532730	NM_002016.2(FLG):c.11177G>C (p.Arg3726Pro)	CCDST, FLG (R3726P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095413	NM_002016.2(FLG):c.11170C>A (p.His3724Asn)	CCDST, FLG (H3724N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2255238	NM_002016.2(FLG):c.11162A>G (p.Glu3721Gly)	CCDST, FLG (E3721G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2265418	NM_002016.2(FLG):c.11101G>A (p.Ala3701Thr)	CCDST, FLG (A3701T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2508951	NM_002016.2(FLG):c.11090G>A (p.Arg3697His)	CCDST, FLG (R3697H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2354641	NM_002016.2(FLG):c.11057G>C (p.Gly3686Ala)	CCDST, FLG (G3686A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095412	NM_002016.2(FLG):c.11056G>A (p.Gly3686Arg)	CCDST, FLG (G3686R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095411	NM_002016.2(FLG):c.11047G>C (p.Gly3683Arg)	CCDST, FLG (G3683R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2383858	NM_002016.2(FLG):c.11047G>A (p.Gly3683Arg)	CCDST, FLG (G3683R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2546117	NM_002016.2(FLG):c.11042C>T (p.Ala3681Val)	CCDST, FLG (A3681V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2393725	NM_002016.2(FLG):c.11042C>G (p.Ala3681Gly)	CCDST, FLG (A3681G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2240015	NM_002016.2(FLG):c.11024A>C (p.Asp3675Ala)	CCDST, FLG (D3675A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2393724	NM_002016.2(FLG):c.11019C>G (p.Asp3673Glu)	CCDST, FLG (D3673E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095410	NM_002016.2(FLG):c.11000G>A (p.Ser3667Asn)	CCDST, FLG (S3667N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2245614	NM_002016.2(FLG):c.10996G>A (p.Asp3666Asn)	CCDST, FLG (D3666N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095409	NM_002016.2(FLG):c.10924A>T (p.Ile3642Phe)	CCDST, FLG (I3642F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095408	NM_002016.2(FLG):c.10907G>A (p.Ser3636Asn)	CCDST, FLG (S3636N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2344668	NM_002016.2(FLG):c.10907G>C (p.Ser3636Thr)	CCDST, FLG (S3636T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492496	NM_002016.2(FLG):c.10890C>G (p.His3630Gln)	CCDST, FLG (H3630Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2290961	NM_002016.2(FLG):c.10886A>G (p.His3629Arg)	CCDST, FLG (H3629R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2378485	NM_002016.2(FLG):c.10872G>C (p.Glu3624Asp)	CCDST, FLG (E3624D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095407	NM_002016.2(FLG):c.10838C>T (p.Ser3613Leu)	CCDST, FLG (S3613L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279102	NM_002016.2(FLG):c.10831G>A (p.Ala3611Thr)	CCDST, FLG (A3611T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2366777	NM_002016.2(FLG):c.10817C>T (p.Ser3606Phe)	CCDST, FLG (S3606F)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2402096	NM_002016.2(FLG):c.10811A>G (p.Glu3604Gly)	CCDST, FLG (E3604G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279094	NM_002016.2(FLG):c.10799C>G (p.Thr3600Ser)	CCDST, FLG (T3600S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2463324	NM_002016.2(FLG):c.10769A>T (p.His3590Leu)	CCDST, FLG (H3590L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095403	NM_002016.2(FLG):c.10765G>A (p.Gly3589Arg)	CCDST, FLG (G3589R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 1049020	NM_002016.2(FLG):c.10747G>A (p.Glu3583Lys)	CCDST, FLG (E3583K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2227747	NM_002016.2(FLG):c.10738T>C (p.Ser3580Pro)	CCDST, FLG (S3580P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2323874	NM_002016.2(FLG):c.10731C>G (p.His3577Gln)	CCDST, FLG (H3577Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095402	NM_002016.2(FLG):c.10717G>C (p.Asp3573His)	CCDST, FLG (D3573H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247345	NM_002016.2(FLG):c.10615G>T (p.Val3539Phe)	CCDST, FLG (V3539F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2474659	NM_002016.2(FLG):c.10583G>C (p.Gly3528Ala)	CCDST, FLG (G3528A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2539547	NM_002016.2(FLG):c.10573C>A (p.Gln3525Lys)	CCDST, FLG (Q3525K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2507623	NM_002016.2(FLG):c.10573C>G (p.Gln3525Glu)	CCDST, FLG (Q3525E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2300957	NM_002016.2(FLG):c.10518C>A (p.His3506Gln)	CCDST, FLG (H3506Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2262401	NM_002016.2(FLG):c.10492G>A (p.Gly3498Ser)	CCDST, FLG (G3498S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2516606	NM_002016.2(FLG):c.10483T>A (p.Ser3495Thr)	CCDST, FLG (S3495T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2395207	NM_002016.2(FLG):c.10477G>A (p.Glu3493Lys)	CCDST, FLG (E3493K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2461460	NM_002016.2(FLG):c.10469G>A (p.Arg3490His)	CCDST, FLG (R3490H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2241075	NM_002016.2(FLG):c.10469G>C (p.Arg3490Pro)	CCDST, FLG (R3490P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095399	NM_002016.2(FLG):c.10466C>T (p.Thr3489Ile)	CCDST, FLG (T3489I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095398	NM_002016.2(FLG):c.10430G>A (p.Arg3477His)	CCDST, FLG (R3477H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3095397	NM_002016.2(FLG):c.10388A>T (p.His3463Leu)	CCDST, FLG (H3463L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279095	NM_002016.2(FLG):c.10368G>C (p.Arg3456Ser)	CCDST, FLG (R3456S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2210245	NM_002016.2(FLG):c.10361T>C (p.Val3454Ala)	CCDST, FLG (V3454A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3095396	NM_002016.2(FLG):c.10351G>A (p.Glu3451Lys)	CCDST, FLG (E3451K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2349141	NM_002016.2(FLG):c.10345C>T (p.His3449Tyr)	CCDST, FLG (H3449Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2353537	NM_002016.2(FLG):c.10335G>C (p.Arg3445Ser)	CCDST, FLG (R3445S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2335631	NM_002016.2(FLG):c.10329A>T (p.Arg3443Ser)	CCDST, FLG (R3443S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2349140	NM_002016.2(FLG):c.10323C>G (p.Ser3441Arg)	CCDST, FLG (S3441R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279097	NM_002016.2(FLG):c.10312C>A (p.Pro3438Thr)	CCDST, FLG (P3438T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279064	NM_002016.2(FLG):c.10287G>C (p.Glu3429Asp)	CCDST, FLG (E3429D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279049	NM_002016.2(FLG):c.10277C>T (p.Ala3426Val)	CCDST, FLG (A3426V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3279124	NM_002016.2(FLG):c.10270C>T (p.His3424Tyr)	CCDST, FLG (H3424Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2384905	NM_002016.2(FLG):c.10259A>G (p.Asp3420Gly)	CCDST, FLG (D3420G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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