ClinVar for Gene (Select 3535) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3335355	NM_080764.4(ZNF280B):c.1086C>T (p.Ile362=)	IGL, ZNF280B	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3335354	NM_080764.4(ZNF280B):c.648T>A (p.Ser216Arg)	IGL, ZNF280B (S216R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335353	NM_080764.4(ZNF280B):c.500A>G (p.Glu167Gly)	IGL, ZNF280B (E167G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335352	NM_080740.5(ZNF280A):c.916G>A (p.Val306Ile)	IGL, ZNF280A (V306I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335351	NM_080740.5(ZNF280A):c.1295T>C (p.Phe432Ser)	IGL, ZNF280A (F432S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335350	NM_080740.5(ZNF280A):c.46A>C (p.Asn16His)	IGL, ZNF280A (N16H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332136	NM_007128.4(VPREB1):c.13C>G (p.Pro5Ala)	IGL, VPREB1 (P5A)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 3332135	NM_007128.4(VPREB1):c.80C>T (p.Pro27Leu)	IGL, VPREB1 (P26L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309663	NM_206956.3(PRAME):c.1293C>G (p.Ile431Met)	IGL, PRAME (I415M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309662	NM_206956.3(PRAME):c.130G>A (p.Ala44Thr)	IGL, PRAME (A28T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285596	NM_001178126.2(IGLL5):c.440C>A (p.Thr147Lys)	IGL, IGLC1 +1 more (T147K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3281341	NM_199127.3(GGTLC2):c.314C>T (p.Pro105Leu)	GGTLC2, IGL (P105L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218133	NM_206956.3(PRAME):c.998G>A (p.Arg333Gln)	IGL, PRAME (R317Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218132	NM_206956.3(PRAME):c.833C>T (p.Pro278Leu)	IGL, PRAME (P262L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218131	NM_206956.3(PRAME):c.82G>A (p.Glu28Lys)	IGL, PRAME (E12K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218130	NM_206956.3(PRAME):c.770G>A (p.Gly257Asp)	IGL, PRAME (G257D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218129	NM_206956.3(PRAME):c.697G>T (p.Asp233Tyr)	IGL, PRAME (D217Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218128	NM_206956.3(PRAME):c.654G>T (p.Met218Ile)	IGL, PRAME (M202I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218127	NM_206956.3(PRAME):c.362T>C (p.Val121Ala)	IGL, PRAME (V105A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218126	NM_206956.3(PRAME):c.1465C>T (p.His489Tyr)	IGL, PRAME (H489Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218125	NM_206956.3(PRAME):c.1426C>T (p.Arg476Trp)	IGL, PRAME (R460W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218124	NM_206956.3(PRAME):c.1304A>G (p.Asn435Ser)	IGL, PRAME (N435S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218123	NM_206956.3(PRAME):c.1020G>A (p.Met340Ile)	IGL, PRAME (M340I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3218122	NM_206956.3(PRAME):c.1009G>C (p.Gly337Arg)	IGL, PRAME (G321R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194865	NM_080764.4(ZNF280B):c.68T>C (p.Val23Ala)	IGL, ZNF280B (V23A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194864	NM_080764.4(ZNF280B):c.310G>T (p.Ala104Ser)	IGL, ZNF280B (A104S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194863	NM_080764.4(ZNF280B):c.1345T>A (p.Cys449Ser)	IGL, ZNF280B (C449S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194862	NM_080764.4(ZNF280B):c.110A>G (p.His37Arg)	IGL, ZNF280B (H37R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194861	NM_080764.4(ZNF280B):c.1031C>G (p.Thr344Ser)	IGL, ZNF280B (T344S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194860	NM_080740.5(ZNF280A):c.982G>A (p.Asp328Asn)	IGL, ZNF280A (D328N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194859	NM_080740.5(ZNF280A):c.746C>T (p.Ala249Val)	IGL, ZNF280A (A249V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194858	NM_080740.5(ZNF280A):c.715C>T (p.Leu239Phe)	IGL, ZNF280A (L239F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194857	NM_080740.5(ZNF280A):c.238C>T (p.Arg80Cys)	IGL, ZNF280A (R80C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194856	NM_080740.5(ZNF280A):c.181A>C (p.Asn61His)	IGL, ZNF280A (N61H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194854	NM_080740.5(ZNF280A):c.1376A>G (p.Gln459Arg)	IGL, ZNF280A (Q459R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194853	NM_080740.5(ZNF280A):c.1219G>A (p.Ala407Thr)	IGL, ZNF280A (A407T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194851	NM_080740.5(ZNF280A):c.1093G>C (p.Val365Leu)	IGL, ZNF280A (V365L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194850	NM_080740.5(ZNF280A):c.1078A>G (p.Met360Val)	IGL, ZNF280A (M360V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194849	NM_080740.5(ZNF280A):c.1021C>T (p.Arg341Trp)	IGL, ZNF280A (R341W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188735	NM_007128.4(VPREB1):c.67C>G (p.Leu23Val)	IGL, VPREB1 (L23V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188734	NM_007128.4(VPREB1):c.388G>C (p.Glu130Gln)	IGL, VPREB1 (E130Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188733	NM_007128.4(VPREB1):c.355G>T (p.Ala119Ser)	IGL, VPREB1 (A118S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188732	NM_007128.4(VPREB1):c.305T>A (p.Ile102Asn)	IGL, VPREB1 (I102N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3188731	NM_007128.4(VPREB1):c.160G>A (p.Val54Ile)	IGL, VPREB1 (V54I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3108767	NM_001178126.2(IGLL5):c.83T>G (p.Leu28Arg)	IGL, IGLL5 (L28R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3108766	NM_001178126.2(IGLL5):c.637T>C (p.Cys213Arg)	IGL, IGLC1 +1 more (C213R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108764	NM_001178126.2(IGLL5):c.587A>G (p.Gln196Arg)	IGL, IGLC1 +1 more (Q121R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108763	NM_001178126.2(IGLL5):c.469G>A (p.Val157Ile)	IGL, IGLC1 +1 more (V157I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3108762	NM_001178126.2(IGLL5):c.427C>T (p.Pro143Ser)	IGL, IGLC1 +1 more (P68S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108761	NM_001178126.2(IGLL5):c.344C>T (p.Pro115Leu)	IGL, IGLC1 +1 more (P40L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108759	NM_001178126.2(IGLL5):c.236C>T (p.Ala79Val)	IGL, IGLL5 (A79V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3099694	NM_199127.3(GGTLC2):c.640G>A (p.Glu214Lys)	GGTLC2, IGL (E214K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099693	NM_199127.3(GGTLC2):c.589G>A (p.Val197Ile)	GGTLC2, IGL (V197I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099692	NM_199127.3(GGTLC2):c.556G>A (p.Ala186Thr)	GGTLC2, IGL (A220T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099691	NM_199127.3(GGTLC2):c.536G>A (p.Arg179Gln)	GGTLC2, IGL (R179Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099690	NM_199127.3(GGTLC2):c.535C>T (p.Arg179Trp)	GGTLC2, IGL (R179W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099689	NM_199127.3(GGTLC2):c.503T>C (p.Ile168Thr)	GGTLC2, IGL (I168T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099688	NM_199127.3(GGTLC2):c.498A>C (p.Arg166Ser)	GGTLC2, IGL (R166S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099687	NM_199127.3(GGTLC2):c.46G>C (p.Asp16His)	GGTLC2, IGL (D16H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099686	NM_199127.3(GGTLC2):c.368G>C (p.Ser123Thr)	GGTLC2, IGL (S123T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099685	NM_199127.3(GGTLC2):c.314C>G (p.Pro105Arg)	GGTLC2, IGL (P105R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099684	NM_199127.3(GGTLC2):c.262G>A (p.Glu88Lys)	GGTLC2, IGL (E88K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099683	NM_199127.3(GGTLC2):c.205A>G (p.Ser69Gly)	GGTLC2, IGL (S69G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3025577	NM_199127.3(GGTLC2):c.176+4G>A	GGTLC2, IGL	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2652956	NM_199127.3(GGTLC2):c.103G>T (p.Gly35Trp)	GGTLC2, IGL (G35W)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2652955	NM_080740.5(ZNF280A):c.48T>C (p.Asn16=)	IGL, ZNF280A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2652954	NM_080740.5(ZNF280A):c.435T>C (p.Thr145=)	IGL, ZNF280A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2652953	NM_080740.5(ZNF280A):c.819C>T (p.Ile273=)	IGL, ZNF280A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2628004	NM_080764.4(ZNF280B):c.937G>A (p.Val313Met)	IGL, ZNF280B (V313M)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2622658	NM_206956.3(PRAME):c.92G>T (p.Gly31Val)	IGL, PRAME (G31V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594520	NM_199127.3(GGTLC2):c.592C>T (p.Arg198Cys)	GGTLC2, IGL (R198C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591552	NM_206956.3(PRAME):c.1510C>T (p.Pro504Ser)	IGL, PRAME (P504S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590819	NM_199127.3(GGTLC2):c.593G>A (p.Arg198His)	GGTLC2, IGL (R232H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570227	NM_199127.3(GGTLC2):c.193C>T (p.Arg65Cys)	GGTLC2, IGL (R65C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2565307	NM_080740.5(ZNF280A):c.1011G>C (p.Gln337His)	IGL, ZNF280A (Q337H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557319	NM_080764.4(ZNF280B):c.290A>G (p.Glu97Gly)	IGL, ZNF280B (E97G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543720	NM_001178126.2(IGLL5):c.323T>C (p.Leu108Pro)	IGL, IGLJ1 +1 more (L108P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536546	NM_199127.3(GGTLC2):c.290A>G (p.Asn97Ser)	GGTLC2, IGL (N97S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535753	NM_206956.3(PRAME):c.1361C>G (p.Thr454Ser)	IGL, PRAME (T454S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535607	NM_080764.4(ZNF280B):c.406A>G (p.Asn136Asp)	IGL, ZNF280B (N136D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535095	NM_080740.5(ZNF280A):c.1544C>T (p.Pro515Leu)	IGL, ZNF280A (P515L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532594	NM_001178126.2(IGLL5):c.610G>A (p.Val204Met)	IGL, IGLC1 +1 more (V129M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531931	NM_007128.4(VPREB1):c.253C>T (p.Pro85Ser)	IGL, VPREB1 (P85S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526556	NM_206956.3(PRAME):c.967C>G (p.Pro323Ala)	IGL, PRAME (P307A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519453	NM_001178126.2(IGLL5):c.445G>A (p.Ala149Thr)	IGL, IGLC1 +1 more (A149T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518718	NM_080764.4(ZNF280B):c.1021A>G (p.Asn341Asp)	IGL, ZNF280B (N341D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516233	NM_080740.5(ZNF280A):c.251C>T (p.Ala84Val)	IGL, ZNF280A (A84V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515707	NM_001178126.2(IGLL5):c.121C>T (p.Pro41Ser)	IGL, IGLL5 (P41S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512782	NM_206956.3(PRAME):c.236C>T (p.Thr79Ile)	IGL, PRAME (T63I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496118	NM_001178126.2(IGLL5):c.104C>T (p.Ala35Val)	IGL, IGLL5 (A35V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495392	NM_080740.5(ZNF280A):c.1553C>G (p.Ser518Cys)	IGL, ZNF280A (S518C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484652	NM_001178126.2(IGLL5):c.179G>C (p.Arg60Pro)	IGL, IGLL5 (R60P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474596	NM_199127.3(GGTLC2):c.601G>T (p.Gly201Cys)	GGTLC2, IGL (G235C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470483	NM_007128.4(VPREB1):c.367G>C (p.Glu123Gln)	IGL, VPREB1 (E123Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464799	NM_080740.5(ZNF280A):c.1211C>T (p.Ser404Leu)	IGL, ZNF280A (S404L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464104	NM_199127.3(GGTLC2):c.389T>C (p.Met130Thr)	GGTLC2, IGL (M130T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462514	NM_080764.4(ZNF280B):c.888A>T (p.Glu296Asp)	IGL, ZNF280B (E296D)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2461322	NM_080740.5(ZNF280A):c.685C>T (p.Pro229Ser)	IGL, ZNF280A (P229S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460160	NM_080740.5(ZNF280A):c.1132G>A (p.Val378Ile)	IGL, ZNF280A (V378I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457980	NM_199127.3(GGTLC2):c.320C>T (p.Ser107Leu)	GGTLC2, IGL (S107L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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