ClinVar for Gene (Select 23140) - ClinVar - NCBI

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

Links from Gene

Items: 1 to 100 of 256

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3260267	NM_015113.4(ZZEF1):c.2975A>G (p.Asp992Gly)	ZZEF1 (D992G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260266	NM_015113.4(ZZEF1):c.3181C>T (p.Leu1061Phe)	ZZEF1 (L1061F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260265	NM_015113.4(ZZEF1):c.5239A>G (p.Met1747Val)	ZZEF1 (M1747V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260264	NM_015113.4(ZZEF1):c.5075A>G (p.Asn1692Ser)	ZZEF1 (N1692S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3260263	NM_015113.4(ZZEF1):c.85G>A (p.Ala29Thr)	ZZEF1 (A29T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260262	NM_015113.4(ZZEF1):c.3889T>G (p.Ser1297Ala)	ZZEF1 (S1297A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260259	NM_015113.4(ZZEF1):c.3664A>T (p.Met1222Leu)	ZZEF1 (M1222L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260258	NM_015113.4(ZZEF1):c.2956G>T (p.Ala986Ser)	ZZEF1 (A986S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260257	NM_015113.4(ZZEF1):c.1598A>G (p.Gln533Arg)	ZZEF1 (Q533R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260256	NM_015113.4(ZZEF1):c.268C>G (p.Arg90Gly)	ZZEF1 (R90G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260255	NM_015113.4(ZZEF1):c.5191G>A (p.Ala1731Thr)	ZZEF1 (A1731T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260254	NM_015113.4(ZZEF1):c.5959G>A (p.Glu1987Lys)	ZZEF1 (E1987K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260253	NM_015113.4(ZZEF1):c.8369A>G (p.Tyr2790Cys)	ZZEF1 (Y2790C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260252	NM_015113.4(ZZEF1):c.8158A>G (p.Ile2720Val)	ZZEF1 (I2720V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260251	NM_015113.4(ZZEF1):c.5369C>T (p.Ala1790Val)	ZZEF1 (A1790V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260250	NM_015113.4(ZZEF1):c.5078A>G (p.Asp1693Gly)	ZZEF1 (D1693G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260248	NM_015113.4(ZZEF1):c.8791C>T (p.Arg2931Cys)	ZZEF1 (R2931C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260247	NM_015113.4(ZZEF1):c.2535C>G (p.Asp845Glu)	ZZEF1 (D845E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260246	NM_015113.4(ZZEF1):c.4487A>G (p.Lys1496Arg)	ZZEF1 (K1496R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260245	NM_015113.4(ZZEF1):c.7319G>A (p.Arg2440Gln)	ZZEF1 (R2440Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260244	NM_015113.4(ZZEF1):c.574C>T (p.Arg192Cys)	ZZEF1 (R192C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260243	NM_015113.4(ZZEF1):c.7900G>A (p.Val2634Met)	ZZEF1 (V2634M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260242	NM_015113.4(ZZEF1):c.2630A>G (p.His877Arg)	ZZEF1 (H877R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260241	NM_015113.4(ZZEF1):c.4551G>T (p.Leu1517Phe)	ZZEF1 (L1517F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260240	NM_015113.4(ZZEF1):c.2099G>A (p.Ser700Asn)	ZZEF1 (S700N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260239	NM_015113.4(ZZEF1):c.2359G>A (p.Val787Ile)	ZZEF1 (V787I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3260238	NM_015113.4(ZZEF1):c.6695A>T (p.Gln2232Leu)	ZZEF1 (Q2232L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260237	NM_015113.4(ZZEF1):c.1927T>A (p.Ser643Thr)	ZZEF1 (S643T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260236	NM_015113.4(ZZEF1):c.2621G>A (p.Arg874Gln)	ZZEF1 (R874Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260235	NM_015113.4(ZZEF1):c.6257A>G (p.Gln2086Arg)	ZZEF1 (Q2086R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260234	NM_015113.4(ZZEF1):c.3994A>T (p.Thr1332Ser)	ZZEF1 (T1332S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260233	NM_015113.4(ZZEF1):c.8743G>A (p.Val2915Met)	ZZEF1 (V2915M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260232	NM_015113.4(ZZEF1):c.3634C>T (p.Arg1212Trp)	ZZEF1 (R1212W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260231	NM_015113.4(ZZEF1):c.6421G>A (p.Gly2141Ser)	ZZEF1 (G2141S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260230	NM_015113.4(ZZEF1):c.8525A>T (p.Gln2842Leu)	ZZEF1 (Q2842L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260229	NM_015113.4(ZZEF1):c.7654C>T (p.Arg2552Cys)	ZZEF1 (R2552C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3243205	NC_000017.10:g.(?_422368)_(8285628_?)dup	FBXO39, FGF11 +209 more	Duplication	not provided	GUncertain significance
Select item 3199775	NM_015113.4(ZZEF1):c.8726G>T (p.Arg2909Leu)	ZZEF1 (R2909L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199773	NM_015113.4(ZZEF1):c.8609C>A (p.Pro2870His)	ZZEF1 (P2870H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199772	NM_015113.4(ZZEF1):c.8578A>G (p.Ser2860Gly)	ZZEF1 (S2860G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199771	NM_015113.4(ZZEF1):c.8495T>C (p.Val2832Ala)	ZZEF1 (V2832A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199770	NM_015113.4(ZZEF1):c.8439G>T (p.Leu2813Phe)	ZZEF1 (L2813F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199769	NM_015113.4(ZZEF1):c.8384C>T (p.Thr2795Met)	ZZEF1 (T2795M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199768	NM_015113.4(ZZEF1):c.8054C>T (p.Ala2685Val)	ZZEF1 (A2685V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199767	NM_015113.4(ZZEF1):c.8047A>T (p.Thr2683Ser)	ZZEF1 (T2683S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199766	NM_015113.4(ZZEF1):c.8041C>G (p.Leu2681Val)	ZZEF1 (L2681V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199765	NM_015113.4(ZZEF1):c.7991A>C (p.Glu2664Ala)	ZZEF1 (E2664A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199764	NM_015113.4(ZZEF1):c.793A>G (p.Ile265Val)	ZZEF1 (I265V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199763	NM_015113.4(ZZEF1):c.7813G>T (p.Asp2605Tyr)	ZZEF1 (D2605Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199762	NM_015113.4(ZZEF1):c.7492G>C (p.Glu2498Gln)	ZZEF1 (E2498Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199760	NM_015113.4(ZZEF1):c.7477G>A (p.Asp2493Asn)	ZZEF1 (D2493N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199759	NM_015113.4(ZZEF1):c.7444C>T (p.Arg2482Trp)	ZZEF1 (R2482W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199758	NM_015113.4(ZZEF1):c.7253A>G (p.Asn2418Ser)	ZZEF1 (N2418S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3199757	NM_015113.4(ZZEF1):c.6739G>A (p.Val2247Met)	ZZEF1 (V2247M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199756	NM_015113.4(ZZEF1):c.6553C>G (p.Leu2185Val)	ZZEF1 (L2185V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199755	NM_015113.4(ZZEF1):c.6400C>T (p.His2134Tyr)	ZZEF1 (H2134Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199754	NM_015113.4(ZZEF1):c.5525G>A (p.Arg1842Gln)	ZZEF1 (R1842Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199753	NM_015113.4(ZZEF1):c.4915G>C (p.Asp1639His)	ZZEF1 (D1639H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199752	NM_015113.4(ZZEF1):c.4735T>C (p.Ser1579Pro)	ZZEF1 (S1579P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199751	NM_015113.4(ZZEF1):c.4197A>C (p.Glu1399Asp)	ZZEF1 (E1399D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199750	NM_015113.4(ZZEF1):c.4049A>T (p.Asp1350Val)	ZZEF1 (D1350V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199749	NM_015113.4(ZZEF1):c.3635G>A (p.Arg1212Gln)	ZZEF1 (R1212Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199748	NM_015113.4(ZZEF1):c.3502G>A (p.Gly1168Ser)	ZZEF1 (G1168S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199747	NM_015113.4(ZZEF1):c.345G>C (p.Gln115His)	ZZEF1 (Q115H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199745	NM_015113.4(ZZEF1):c.3205T>C (p.Cys1069Arg)	ZZEF1 (C1069R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199744	NM_015113.4(ZZEF1):c.3199A>C (p.Lys1067Gln)	ZZEF1 (K1067Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199743	NM_015113.4(ZZEF1):c.3068A>G (p.Glu1023Gly)	ZZEF1 (E1023G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199742	NM_015113.4(ZZEF1):c.3012C>A (p.Ser1004Arg)	ZZEF1 (S1004R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199741	NM_015113.4(ZZEF1):c.2905G>A (p.Gly969Ser)	ZZEF1 (G969S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199740	NM_015113.4(ZZEF1):c.2892C>G (p.Phe964Leu)	ZZEF1 (F964L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199739	NM_015113.4(ZZEF1):c.2809G>A (p.Val937Ile)	ZZEF1 (V937I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199738	NM_015113.4(ZZEF1):c.2612G>A (p.Arg871Gln)	ZZEF1 (R871Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199736	NM_015113.4(ZZEF1):c.2140G>A (p.Val714Ile)	ZZEF1 (V714I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3199735	NM_015113.4(ZZEF1):c.1937T>C (p.Leu646Pro)	ZZEF1 (L646P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199734	NM_015113.4(ZZEF1):c.1720A>C (p.Thr574Pro)	ZZEF1 (T574P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199733	NM_015113.4(ZZEF1):c.1627A>C (p.Lys543Gln)	ZZEF1 (K543Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199732	NM_015113.4(ZZEF1):c.1538T>C (p.Met513Thr)	ZZEF1 (M513T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199731	NM_015113.4(ZZEF1):c.1341C>G (p.Phe447Leu)	ZZEF1 (F447L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199730	NM_015113.4(ZZEF1):c.1196A>G (p.Tyr399Cys)	ZZEF1 (Y399C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063486	GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3	ABR, ACADVL +329 more	Copy number gain	not specified	GPathogenic
Select item 3063485	GRCh37/hg19 17p13.3-13.2(chr17:9474-6017500)x1	ABR, ALOX15 +116 more	Copy number loss	not specified	GPathogenic
Select item 2681682	NM_015113.4(ZZEF1):c.7825C>T (p.Arg2609Ter)	ZZEF1 (R2609*)	Single nucleotide variant (nonsense)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2671597	Single allele	ABR, ALOX15 +80 more	Deletion	not provided	GPathogenic
Select item 2647251	NM_015113.4(ZZEF1):c.204C>T (p.Pro68=)	ZZEF1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2647250	NM_015113.4(ZZEF1):c.764A>G (p.Tyr255Cys)	ZZEF1 (Y255C)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2647249	NM_015113.4(ZZEF1):c.2901C>T (p.Val967=)	ZZEF1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2647248	NM_015113.4(ZZEF1):c.3156C>T (p.Cys1052=)	ZZEF1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2647247	NM_015113.4(ZZEF1):c.3217G>A (p.Glu1073Lys)	ZZEF1 (E1073K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2647246	NM_015113.4(ZZEF1):c.5934A>T (p.Pro1978=)	ZZEF1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2647245	NM_015113.4(ZZEF1):c.8496G>A (p.Val2832=)	ZZEF1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2621474	NM_015113.4(ZZEF1):c.5387G>A (p.Arg1796His)	ZZEF1 (R1796H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620680	NM_015113.4(ZZEF1):c.7712C>G (p.Thr2571Arg)	ZZEF1 (T2571R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619834	NM_015113.4(ZZEF1):c.2054G>A (p.Arg685His)	ZZEF1 (R685H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619515	NM_015113.4(ZZEF1):c.3157G>A (p.Val1053Met)	ZZEF1 (V1053M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617041	NM_015113.4(ZZEF1):c.7280A>G (p.Glu2427Gly)	ZZEF1 (E2427G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608318	NM_015113.4(ZZEF1):c.2402T>C (p.Phe801Ser)	ZZEF1 (F801S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605236	NM_015113.4(ZZEF1):c.7904C>T (p.Pro2635Leu)	ZZEF1 (P2635L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601208	NM_015113.4(ZZEF1):c.1364A>G (p.Glu455Gly)	ZZEF1 (E455G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600144	NM_015113.4(ZZEF1):c.6407C>T (p.Thr2136Ile)	ZZEF1 (T2136I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597947	NM_015113.4(ZZEF1):c.5807G>A (p.Arg1936Gln)	ZZEF1 (R1936Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 3