Related gene-specific medical variations for Gene (Select 1540) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3370156	NM_001378743.1(CYLD):c.1949+5G>A	CYLD, CYLD-AS2	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3364289	NM_001378743.1(CYLD):c.2273G>A (p.Arg758Gln)	CYLD, CYLD-AS2 (R533Q +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3360386	NM_001378743.1(CYLD):c.254A>T (p.Asp85Val)	CYLD (D85V)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3350639	NM_001378743.1(CYLD):c.2390A>G (p.Tyr797Cys)	CYLD, CYLD-AS2 (Y572C +3 more)	Single nucleotide variant (missense variant +1 more)	CYLD-related disorder	GLikely benign
Select item 3258010	NM_001378743.1(CYLD):c.2344_2350+1del	CYLD, CYLD-AS2	Deletion (splice donor variant)	Neoplasm	OLikely oncogenic
Select item 3243651	NC_000016.9:g.(?_50820746)_(50821783_?)del	CYLD	Deletion	not provided	GUncertain significance
Select item 3241259	NM_001378743.1(CYLD):c.228G>C (p.Glu76Asp)	CYLD (E76D)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241258	NM_001378743.1(CYLD):c.730A>G (p.Ile244Val)	CYLD (I22V +1 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241257	NM_001378743.1(CYLD):c.676G>A (p.Glu226Lys)	CYLD (E226K +1 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241256	NM_001378743.1(CYLD):c.2482C>T (p.Pro828Ser)	CYLD, CYLD-AS2 (P603S +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241255	NM_001378743.1(CYLD):c.2512G>A (p.Val838Met)	CYLD, CYLD-AS2 (V613M +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241254	NM_001378743.1(CYLD):c.895A>G (p.Ile299Val)	CYLD (I299V +1 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241253	NM_001378743.1(CYLD):c.1949T>A (p.Ile650Lys)	CYLD, CYLD-AS2 (I425K +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241252	NM_001378743.1(CYLD):c.98A>G (p.Lys33Arg)	CYLD (K33R)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241251	NM_001378743.1(CYLD):c.1121C>T (p.Thr374Ile)	CYLD (T149I +2 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241250	NM_001378743.1(CYLD):c.2495A>G (p.Asn832Ser)	CYLD, CYLD-AS2 (N607S +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241249	NM_001378743.1(CYLD):c.2426C>T (p.Ser809Leu)	CYLD, CYLD-AS2 (S584L +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241248	NM_001378743.1(CYLD):c.2678A>G (p.Asp893Gly)	CYLD, CYLD-AS2 (D668G +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241247	NM_001378743.1(CYLD):c.1724C>T (p.Thr575Ile)	CYLD (T350I +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241246	NM_001378743.1(CYLD):c.829G>A (p.Asp277Asn)	CYLD (D277N +1 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241245	NM_001378743.1(CYLD):c.2570A>T (p.Gln857Leu)	CYLD-AS2, CYLD (Q632L +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241244	NM_001378743.1(CYLD):c.2554G>A (p.Gly852Ser)	CYLD, CYLD-AS2 (G627S +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241243	NM_001378743.1(CYLD):c.2512G>C (p.Val838Leu)	CYLD, CYLD-AS2 (V613L +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241242	NM_001378743.1(CYLD):c.2410G>A (p.Asp804Asn)	CYLD, CYLD-AS2 (D579N +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241241	NM_001378743.1(CYLD):c.190A>G (p.Lys64Glu)	CYLD (K64E)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241240	NM_001378743.1(CYLD):c.2119C>A (p.Gln707Lys)	CYLD, CYLD-AS2 (Q482K +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241239	NM_001378743.1(CYLD):c.335T>A (p.Leu112Gln)	CYLD (L112Q)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241238	NM_001378743.1(CYLD):c.305C>T (p.Ala102Val)	CYLD (A102V)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241237	NM_001378743.1(CYLD):c.2538C>A (p.Asp846Glu)	CYLD, CYLD-AS2 (D621E +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241236	NM_001378743.1(CYLD):c.284A>G (p.Lys95Arg)	CYLD (K95R)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241235	NM_001378743.1(CYLD):c.1208A>C (p.Gln403Pro)	CYLD (Q178P +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241234	NM_001378743.1(CYLD):c.522A>C (p.Gln174His)	CYLD (Q174H)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241233	NM_001378743.1(CYLD):c.1435A>G (p.Lys479Glu)	CYLD (K254E +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241232	NM_001378743.1(CYLD):c.1087G>C (p.Val363Leu)	CYLD (V138L +2 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241231	NM_001378743.1(CYLD):c.1882A>G (p.Asn628Asp)	CYLD, CYLD-AS2 (N403D +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3241230	NM_001378743.1(CYLD):c.2242G>A (p.Ala748Thr)	CYLD, CYLD-AS2 (A523T +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 3069095	NM_001378743.1(CYLD):c.2390A>T (p.Tyr797Phe)	CYLD, CYLD-AS2 (Y572F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3068572	NM_001378743.1(CYLD):c.2039A>G (p.Lys680Arg)	CYLD, CYLD-AS2 (K455R +3 more)	Single nucleotide variant (missense variant +1 more)	Familial cylindromatosis	GUncertain significance
Select item 3047958	NM_001378743.1(CYLD):c.2553C>T (p.His851=)	CYLD, CYLD-AS2	Single nucleotide variant (synonymous variant +1 more)	CYLD-related disorder	GLikely benign
Select item 3038656	NM_001378743.1(CYLD):c.2282_2283del (p.Lys761fs)	CYLD, CYLD-AS2 (K536fs +3 more)	Deletion (frameshift variant +1 more)	CYLD-related disorder	GLikely pathogenic
Select item 3037023	NM_001378743.1(CYLD):c.2340A>G (p.Leu780=)	CYLD, CYLD-AS2	Single nucleotide variant (synonymous variant +1 more)	CYLD-related disorder	GLikely benign
Select item 3034171	NM_001378743.1(CYLD):c.2475C>T (p.His825=)	CYLD, CYLD-AS2	Single nucleotide variant (synonymous variant +1 more)	CYLD-related disorder	GLikely benign
Select item 3032767	NM_001378743.1(CYLD):c.1985T>C (p.Leu662Pro)	CYLD, CYLD-AS2 (L437P +3 more)	Single nucleotide variant (missense variant +1 more)	CYLD-related disorder	GUncertain significance
Select item 3025155	NM_001378743.1(CYLD):c.2148A>G (p.Gln716=)	CYLD, CYLD-AS2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2956906	NM_001378743.1(CYLD):c.2109-11C>T	CYLD, CYLD-AS2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2878002	NM_001378743.1(CYLD):c.2385A>C (p.Ala795=)	CYLD, CYLD-AS2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2681079	NM_001378743.1(CYLD):c.1111del (p.Ser371fs)	CYLD (S146fs +2 more)	Deletion (frameshift variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GLikely pathogenic
Select item 2681078	NM_001378743.1(CYLD):c.680T>C (p.Leu227Pro)	CYLD (L227P +1 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681077	NM_001378743.1(CYLD):c.956T>G (p.Leu319Arg)	CYLD (L316R +2 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681076	NM_001378743.1(CYLD):c.694A>G (p.Ile232Val)	CYLD (I10V +1 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681075	NM_001378743.1(CYLD):c.1008A>C (p.Lys336Asn)	CYLD (K111N +2 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681074	NM_001378743.1(CYLD):c.70C>T (p.Leu24Phe)	CYLD (L24F)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681073	NM_001378743.1(CYLD):c.1151C>T (p.Pro384Leu)	CYLD (P159L +2 more)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681072	NM_001378743.1(CYLD):c.611T>C (p.Leu204Pro)	CYLD (L204P)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681071	NM_001378743.1(CYLD):c.761T>G (p.Val254Gly)	CYLD (V254G +1 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681070	NM_001378743.1(CYLD):c.1190G>A (p.Arg397His)	CYLD (R172H +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681068	NM_001378743.1(CYLD):c.421A>C (p.Lys141Gln)	CYLD (K141Q)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681067	NM_001378743.1(CYLD):c.274A>G (p.Ile92Val)	CYLD (I92V)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681066	NM_001378743.1(CYLD):c.1402C>T (p.His468Tyr)	CYLD (H243Y +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681065	NM_001378743.1(CYLD):c.1289A>G (p.Asn430Ser)	CYLD (N205S +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681064	NM_001378743.1(CYLD):c.649G>A (p.Ala217Thr)	CYLD (A217T)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681063	NM_001378743.1(CYLD):c.841G>A (p.Asp281Asn)	CYLD (D281N +1 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681062	NM_001378743.1(CYLD):c.285G>C (p.Lys95Asn)	CYLD (K95N)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681061	NM_001378743.1(CYLD):c.2172A>C (p.Lys724Asn)	CYLD, CYLD-AS2 (K499N +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681060	NM_001378743.1(CYLD):c.1249C>T (p.His417Tyr)	CYLD (H192Y +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681059	NM_001378743.1(CYLD):c.1078G>C (p.Gly360Arg)	CYLD (G135R +2 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681058	NM_001378743.1(CYLD):c.467G>A (p.Arg156Lys)	CYLD (R156K)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681057	NM_001378743.1(CYLD):c.685C>T (p.Pro229Ser)	CYLD (P229S +1 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681056	NM_001378743.1(CYLD):c.640A>G (p.Ser214Gly)	CYLD (S214G)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681055	NM_001378743.1(CYLD):c.1433T>C (p.Val478Ala)	CYLD (V253A +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681054	NM_001378743.1(CYLD):c.241G>T (p.Val81Phe)	CYLD (V81F)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681053	NM_001378743.1(CYLD):c.2644G>A (p.Asp882Asn)	CYLD, CYLD-AS2 (D657N +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681052	NM_001378743.1(CYLD):c.1331C>G (p.Ser444Cys)	CYLD (S219C +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681051	NM_001378743.1(CYLD):c.2434A>G (p.Lys812Glu)	CYLD, CYLD-AS2 (K587E +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681050	NM_001378743.1(CYLD):c.608A>C (p.Glu203Ala)	CYLD (E203A)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681049	NM_001378743.1(CYLD):c.1763T>C (p.Ile588Thr)	CYLD (I363T +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681048	NM_001378743.1(CYLD):c.2650G>T (p.Ala884Ser)	CYLD, CYLD-AS2 (A659S +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681047	NM_001378743.1(CYLD):c.2578G>C (p.Glu860Gln)	CYLD, CYLD-AS2 (E635Q +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681045	NM_001378743.1(CYLD):c.727A>G (p.Thr243Ala)	CYLD (T21A +1 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681044	NM_001378743.1(CYLD):c.1016C>T (p.Ala339Val)	CYLD (A114V +2 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681043	NM_001378743.1(CYLD):c.125C>T (p.Pro42Leu)	CYLD (P42L)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681042	NM_001378743.1(CYLD):c.157C>T (p.Arg53Cys)	CYLD (R53C)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681041	NM_001378743.1(CYLD):c.1141G>T (p.Ala381Ser)	CYLD (A156S +2 more)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681040	NM_001378743.1(CYLD):c.439C>T (p.Arg147Cys)	CYLD (R147C)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681039	NM_001378743.1(CYLD):c.1827-3C>A	CYLD, CYLD-AS2	Single nucleotide variant (intron variant)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681038	NM_001378743.1(CYLD):c.2462A>G (p.Asn821Ser)	CYLD, CYLD-AS2 (N596S +3 more)	Single nucleotide variant (missense variant +1 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2681037	NM_001378743.1(CYLD):c.55C>T (p.Arg19Trp)	CYLD (R19W)	Single nucleotide variant (missense variant +2 more)	Frontotemporal dementia and/or amyotrophic lateral sclerosis 8	GUncertain significance
Select item 2646521	NM_001378743.1(CYLD):c.2814G>A (p.Leu938=)	CYLD-AS2, CYLD	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2646520	NM_001378743.1(CYLD):c.2646T>C (p.Asp882=)	CYLD, CYLD-AS2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2646519	NM_001378743.1(CYLD):c.2476C>T (p.Leu826Phe)	CYLD, CYLD-AS2 (L601F +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2646518	NM_001378743.1(CYLD):c.2418G>A (p.Pro806=)	CYLD, CYLD-AS2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2633029	NM_001378743.1(CYLD):c.2263C>T (p.Gln755Ter)	CYLD, CYLD-AS2 (Q530* +3 more)	Single nucleotide variant (nonsense +1 more)	CYLD-related disorder	GPathogenic
Select item 2617157	NM_001378743.1(CYLD):c.2844G>T (p.Gln948His)	CYLD, CYLD-AS2 (Q945H +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2615954	NM_001378743.1(CYLD):c.2646T>A (p.Asp882Glu)	CYLD, CYLD-AS2 (D879E +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2572901	NM_001378743.1(CYLD):c.2402A>T (p.Glu801Val)	CYLD, CYLD-AS2 (E576V +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2490455	NM_001378743.1(CYLD):c.2516C>T (p.Ser839Leu)	CYLD, CYLD-AS2 (S614L +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2445310	NM_001378743.1(CYLD):c.1189C>A (p.Arg397Ser)	CYLD (R172S +3 more)	Single nucleotide variant (missense variant +1 more)	Ovarian cancer	GBenign
Select item 2445285	NM_001378743.1(CYLD):c.1004A>G (p.Asn335Ser)	CYLD (N110S +2 more)	Single nucleotide variant (missense variant +1 more)	Ovarian cancer	GBenign
Select item 2440669	NM_001378743.1(CYLD):c.1142C>T (p.Ala381Val)	CYLD (A156V +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1803149	NM_001378743.1(CYLD):c.2723dup (p.Cys909fs)	CYLD, CYLD-AS2 (C684fs +3 more)	Duplication (frameshift variant +1 more)	Brooke-Spiegler syndrome	GLikely pathogenic

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