Related gene-specific medical variations for Gene (Select 199713) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3300109	NM_001127255.2(NLRP7):c.2226C>G (p.Ile742Met)	NCR1, NLRP7 (I714M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3300104	NM_001127255.2(NLRP7):c.2008C>G (p.Leu670Val)	NCR1, NLRP7 (L670V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 3235890	NM_001127255.2(NLRP7):c.2585G>A (p.Gly862Glu)	NCR1, NLRP7 (G834E +1 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GLikely pathogenic
Select item 3200702	NM_001127255.2(NLRP7):c.3018G>C (p.Lys1006Asn)	NCR1, NLRP7 (K1006N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3200701	NM_001127255.2(NLRP7):c.2704G>A (p.Ala902Thr)	NCR1, NLRP7 (A874T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3200700	NM_001127255.2(NLRP7):c.2681A>G (p.Tyr894Cys)	NCR1, NLRP7 (Y894C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3048430	NM_001127255.2(NLRP7):c.2364C>T (p.Asn788=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	NLRP7-related disorder	GLikely benign
Select item 3043555	NM_001127255.2(NLRP7):c.2542C>T (p.Leu848=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	NLRP7-related disorder	GLikely benign
Select item 3025641	NM_001127255.2(NLRP7):c.2937C>T (p.Leu979=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3025285	NM_001127255.2(NLRP7):c.2444G>A (p.Arg815His)	NCR1, NLRP7 (R787H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2650496	NM_001127255.2(NLRP7):c.3069T>C (p.Asn1023=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2635805	NM_001127255.2(NLRP7):c.2808dup (p.Arg937fs)	NCR1, NLRP7 (R909fs +1 more)	Duplication (frameshift variant)	NLRP7-related disorder	GLikely pathogenic
Select item 2610862	NM_001127255.2(NLRP7):c.1976G>A (p.Arg659His)	NCR1, NLRP7 (R659H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2604243	NM_001127255.2(NLRP7):c.2551C>G (p.Leu851Val)	NCR1, NLRP7 (L823V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2585388	NM_001127255.2(NLRP7):c.2002T>C (p.Cys668Arg)	NCR1, NLRP7 (C668R)	Single nucleotide variant (missense variant +1 more)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 2571601	NM_001127255.2(NLRP7):c.277+1G>A	NLRP7	Single nucleotide variant (splice donor variant)	Hydatidiform mole, recurrent, 1	GLikely pathogenic
Select item 2557448	NM_001127255.2(NLRP7):c.2717C>A (p.Thr906Lys)	NCR1, NLRP7 (T878K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2434382	NM_001127255.2(NLRP7):c.637A>G (p.Lys213Glu)	NLRP7 (K213E)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 2397043	NM_001127255.2(NLRP7):c.3030A>C (p.Glu1010Asp)	NCR1, NLRP7 (E1010D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2368077	NM_001127255.2(NLRP7):c.2162G>T (p.Arg721Leu)	NCR1, NLRP7 (R721L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2365099	NM_001127255.2(NLRP7):c.2105G>A (p.Ser702Asn)	NCR1, NLRP7 (S674N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2362816	NM_001127255.2(NLRP7):c.2155G>A (p.Ala719Thr)	NCR1, NLRP7 (A719T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2326826	NM_001127255.2(NLRP7):c.2439G>C (p.Met813Ile)	NCR1, NLRP7 (M785I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2302393	NM_001127255.2(NLRP7):c.2654G>A (p.Cys885Tyr)	NCR1, NLRP7 (C857Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2253982	NM_001127255.2(NLRP7):c.2485C>T (p.Arg829Cys)	NCR1, NLRP7 (R801C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2218924	NM_001127255.2(NLRP7):c.2806C>A (p.Leu936Ile)	NCR1, NLRP7 (L908I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2211470	NM_001127255.2(NLRP7):c.2995G>A (p.Glu999Lys)	NCR1, NLRP7 (E971K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2207880	NM_001127255.2(NLRP7):c.2803C>T (p.His935Tyr)	NCR1, NLRP7 (H907Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2206406	NM_001127255.2(NLRP7):c.2453A>G (p.His818Arg)	NCR1, NLRP7 (H818R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 997712	NM_001127255.2(NLRP7):c.2982-28del	NCR1, NLRP7	Deletion (intron variant)	Hydatidiform mole	GLikely benign
Select item 997711	NM_001127255.2(NLRP7):c.2811-23A>G	NCR1, NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole	GBenign
Select item 997710	NM_001127255.2(NLRP7):c.2695C>T (p.Leu899Phe)	NCR1, NLRP7 (L871F +1 more)	Single nucleotide variant (missense variant)	Hydatidiform mole	GUncertain significance
Select item 997709	NM_001127255.2(NLRP7):c.2642+17TG[6]	NCR1, NLRP7	Microsatellite (intron variant)	Hydatidiform mole	GUncertain significance
Select item 894777	NM_001127255.2(NLRP7):c.2250G>C (p.Leu750=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 894776	NM_001127255.2(NLRP7):c.2361C>T (p.Ala787=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 894775	NM_001127255.2(NLRP7):c.2383C>T (p.Arg795Cys)	NCR1, NLRP7 (R795C +1 more)	Single nucleotide variant (missense variant)	NLRP7-related disorder +1 more	GBenign/Likely benign
Select item 894774	NM_001127255.2(NLRP7):c.2420T>G (p.Met807Arg)	NCR1, NLRP7 (M779R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 894773	NM_001127255.2(NLRP7):c.2504G>T (p.Cys835Phe)	NCR1, NLRP7 (C807F +1 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 893861	NM_001127255.2(NLRP7):c.2706C>T (p.Ala902=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1 +1 more	GBenign/Likely benign
Select item 893860	NM_001127255.2(NLRP7):c.2721C>T (p.Asn907=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1	GLikely benign
Select item 893572	NM_001127255.2(NLRP7):c.3031G>C (p.Val1011Leu)	NCR1, NLRP7 (V1011L +2 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 893571	NM_001127255.2(NLRP7):c.3068A>G (p.Asn1023Ser)	NCR1, NLRP7 (N966S +2 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 893570	NM_001127255.2(NLRP7):c.3076G>A (p.Gly1026Arg)	NCR1, NLRP7 (G998R +2 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 893569	NM_001127255.2(NLRP7):c.3082A>G (p.Thr1028Ala)	NCR1, NLRP7 (T1000A +2 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GLikely benign
Select item 893568	NM_206828.4(NLRP7):c.*20C>T	NCR1, NLRP7	Single nucleotide variant	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 892802	NM_001127255.2(NLRP7):c.2154C>T (p.Thr718=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 892801	NM_001127255.2(NLRP7):c.2204A>G (p.His735Arg)	NCR1, NLRP7 (H707R +1 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 892800	NM_001127255.2(NLRP7):c.2226C>T (p.Ile742=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 892762	NM_206828.4(NLRP7):c.*44G>A	NCR1, NLRP7	Single nucleotide variant	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 834074	NM_001127255.2(NLRP7):c.2402T>C (p.Leu801Pro)	NCR1, NLRP7 (L773P +1 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 830330	NM_001127255.2(NLRP7):c.2320_2321insT (p.Thr774Ilefs)	NCR1, NLRP7 (T746fs +1 more)	Insertion (frameshift variant)	Hydatidiform mole, recurrent, 1	GLikely pathogenic
Select item 775585	NM_001127255.2(NLRP7):c.2201C>T (p.Thr734Met)	NCR1, NLRP7 (T734M +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 631820	NM_001127255.2(NLRP7):c.2130-2A>G	NCR1, NLRP7	Single nucleotide variant (splice acceptor variant)	Hydatidiform mole, recurrent, 1 +1 more	GConflicting classifications of pathogenicity
Select item 330163	NM_001127255.2(NLRP7):c.2129+6T>C	NCR1, NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	GBenign
Select item 330162	NM_001127255.2(NLRP7):c.2325G>A (p.Pro775=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1	GLikely benign
Select item 330161	NM_001127255.2(NLRP7):c.2373G>A (p.Leu791=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 330160	NM_001127255.2(NLRP7):c.2384G>A (p.Arg795His)	NCR1, NLRP7 (R795H +1 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1 +1 more	GConflicting classifications of pathogenicity
Select item 330159	NM_001127255.2(NLRP7):c.2548C>T (p.His850Tyr)	NCR1, NLRP7 (H850Y +1 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 330158	NM_001127255.2(NLRP7):c.2682T>C (p.Tyr894=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1 +2 more	GBenign
Select item 330157	NM_001127255.2(NLRP7):c.2750G>A (p.Arg917His)	NCR1, NLRP7 (R917H +1 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1 +1 more	GUncertain significance
Select item 330156	NM_001127255.2(NLRP7):c.2775A>G (p.Ala925=)	NCR1, NLRP7	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 330155	NM_001127255.2(NLRP7):c.3083C>T (p.Thr1028Met)	NCR1, NLRP7 (T971M +2 more)	Single nucleotide variant (missense variant)	Hydatidiform mole, recurrent, 1 +1 more	GUncertain significance
Select item 330154	NM_206828.4(NLRP7):c.*5C>T	NCR1, NLRP7	Single nucleotide variant	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 330153	NM_206828.4(NLRP7):c.*180G>C	NCR1, NLRP7	Single nucleotide variant	Hydatidiform mole, recurrent, 1	GLikely benign
Select item 330152	NM_206828.4(NLRP7):c.*183G>A	NCR1, NLRP7	Single nucleotide variant	Hydatidiform mole, recurrent, 1	GUncertain significance
Select item 290323	NM_001127255.2(NLRP7):c.2788A>T (p.Asn930Tyr)	NCR1, NLRP7 (N902Y +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 127262	NM_001127255.2(NLRP7):c.516C>T (p.Tyr172=)	NLRP7	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 127261	NM_001127255.2(NLRP7):c.446A>G (p.Asp149Gly)	NLRP7 (D149G)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 127259	NM_001127255.2(NLRP7):c.1461G>A (p.Gly487=)	NLRP7	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 127258	NM_001127255.2(NLRP7):c.1235T>C (p.Leu412Pro)	NLRP7 (L412P)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 127257	NM_001127255.2(NLRP7):c.1171A>G (p.Thr391Ala)	NLRP7 (T391A)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 127256	NM_001127255.2(NLRP7):c.1148C>T (p.Pro383Leu)	NLRP7 (P383L)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 127255	NM_001127255.2(NLRP7):c.1080C>A (p.Gly360=)	NLRP7	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 127254	NM_001127255.2(NLRP7):c.-39-4C>G	NLRP7	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 127253	NM_001127255.1(NLRP7):c.-213G>T	NLRP7	Single nucleotide variant (genic upstream transcript variant)	not provided	Gnot provided
Select item 127252	NM_001127255.1(NLRP7):c.-123C>T	NLRP7	Single nucleotide variant (genic upstream transcript variant)	not provided	Gnot provided
Select item 97901	NM_001127255.2(NLRP7):c.2811-28C>T	NCR1, NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97900	NM_001127255.2(NLRP7):c.-40+36C>T	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97899	NM_001127255.2(NLRP7):c.-40+21C>T	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97898	NM_001127255.2(NLRP7):c.-39-90G>C	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97897	NM_001127255.2(NLRP7):c.-39-792C>T	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97896	NM_001127255.2(NLRP7):c.-39-393G>A	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97895	NM_001127255.2(NLRP7):c.-39-300C>T	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97808	NM_001127255.2(NLRP7):c.985A>C (p.Arg329=)	NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97806	NM_001127255.2(NLRP7):c.915A>C (p.Ala305=)	NLRP7	Single nucleotide variant (synonymous variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97803	NM_001127255.2(NLRP7):c.352+230C>T	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97802	NM_001127255.2(NLRP7):c.353-216C>G	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97801	NM_001127255.2(NLRP7):c.353-178A>G	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97800	NM_001127255.2(NLRP7):c.353-111C>T	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97799	NM_001127255.2(NLRP7):c.352+231G>A	NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97797	NM_001127255.2(NLRP7):c.346A>T (p.Lys116Ter)	NLRP7 (K116*)	Single nucleotide variant (nonsense)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97795	NM_001127255.2(NLRP7):c.2981+33T>G	NCR1, NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97794	NM_001127255.2(NLRP7):c.2981+29_2981+32del	NCR1, NLRP7	Deletion (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97793	NM_001127255.2(NLRP7):c.2981+142C>A	NCR1, NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97792	NM_001127255.2(NLRP7):c.2981+123T>C	NCR1, NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97791	NM_001127255.2(NLRP7):c.295G>T (p.Glu99Ter)	NLRP7 (E99*)	Single nucleotide variant (nonsense)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97790	NM_001127255.2(NLRP7):c.2891T>C (p.Leu964Pro)	NCR1, NLRP7 (L964P +1 more)	Single nucleotide variant (missense variant +1 more)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97789	NM_001127255.2(NLRP7):c.2811-695T>C	NCR1, NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97788	NM_001127255.2(NLRP7):c.2811-678C>A	NCR1, NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided
Select item 97787	NM_001127255.2(NLRP7):c.2811-559A>G	NCR1, NLRP7	Single nucleotide variant (intron variant)	Hydatidiform mole, recurrent, 1	Gnot provided

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