ClinVar Miner

List of variants in gene CYLD reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_001378743.1(CYLD):c.1139-424T>C rs6500332 0.99337
NM_001378743.1(CYLD):c.2469+26A>G rs2302759 0.84878
NM_001378743.1(CYLD):c.1827-308A>G rs8062540 0.37206
NM_001378743.1(CYLD):c.1826+283C>T rs17314341 0.35254
NM_001378743.1(CYLD):c.1138+112G>A rs16948813 0.12089
NM_001378743.1(CYLD):c.2242-46G>T rs10451132 0.11696
NM_001378743.1(CYLD):c.1519-286A>T rs73584482 0.07264
NM_001378743.1(CYLD):c.1518+42G>A rs17222902 0.06711
NM_001378743.1(CYLD):c.2412C>T (p.Asp804=) rs2066852 0.05803
NM_001378743.1(CYLD):c.-123-59A>G rs7187352 0.05692
NM_001378743.1(CYLD):c.2351-240A>G rs73584492 0.05514
NM_001378743.1(CYLD):c.2109-10G>A rs11865799 0.05482
NM_001378743.1(CYLD):c.2041+110G>A rs12599914 0.03907
NM_001378743.1(CYLD):c.1685-115A>C rs74019603 0.03709
NM_001378743.1(CYLD):c.1022-229G>A rs73584479 0.03467
NM_001378743.1(CYLD):c.2350+326G>A rs75157714 0.01766
NM_001378743.1(CYLD):c.1685-86A>G rs7192397 0.01684
NM_001378743.1(CYLD):c.914-161A>G rs112350689 0.01583
NM_001378743.1(CYLD):c.2469+234T>C rs7194167 0.01355
NM_001378743.1(CYLD):c.913+31G>A rs78544610 0.01280
NM_001378743.1(CYLD):c.807+169C>G rs7200535 0.01239
NM_001378743.1(CYLD):c.87C>T (p.Ser29=) rs34564491 0.01188
NM_001378743.1(CYLD):c.2042-50G>A rs113872222 0.01186
NM_001378743.1(CYLD):c.1139-365G>A rs115805200 0.00840
NM_001378743.1(CYLD):c.1473C>T (p.Ile491=) rs75757530 0.00802
NM_001378743.1(CYLD):c.2687-225T>C rs184250395 0.00442
NM_001378743.1(CYLD):c.1518+74C>G rs73584480 0.00377
NM_001378743.1(CYLD):c.2108+51T>C rs368638871 0.00354
NM_001378743.1(CYLD):c.505-159A>G rs117148151 0.00347
NM_001378743.1(CYLD):c.1356A>G (p.Ala452=) rs200886685 0.00107
NM_001378743.1(CYLD):c.59T>G (p.Ile20Ser) rs764097337 0.00005
NM_001378743.1(CYLD):c.635T>C (p.Leu212Ser) rs375434282 0.00002
NM_001378743.1(CYLD):c.932C>T (p.Thr311Met) rs200271412 0.00002
NM_001378743.1(CYLD):c.1112C>A (p.Ser371Ter) rs886040872 0.00001
NM_001378743.1(CYLD):c.1022-264T>A rs78636108
NM_001378743.1(CYLD):c.1681_1682del (p.Leu561fs) rs1597055529
NM_001378743.1(CYLD):c.1684+110C>T rs1420871
NM_001378743.1(CYLD):c.176G>A (p.Arg59Lys) rs2506778799
NM_001378743.1(CYLD):c.1826+60GT[9] rs533669286
NM_001378743.1(CYLD):c.1853A>T (p.Asp618Val) rs2151006616
NM_001378743.1(CYLD):c.1949+5G>A
NM_001378743.1(CYLD):c.1950-82dup rs369024987
NM_001378743.1(CYLD):c.2241+41T>A rs60845592
NM_001378743.1(CYLD):c.2272C>T (p.Arg758Ter) rs121908388
NM_001378743.1(CYLD):c.2273G>A (p.Arg758Gln)
NM_001378743.1(CYLD):c.2402A>T (p.Glu801Val) rs756631851
NM_001378743.1(CYLD):c.2469+274_2470-273dup rs34233862
NM_001378743.1(CYLD):c.2470-273dup rs34233862
NM_001378743.1(CYLD):c.254A>T (p.Asp85Val)
NM_001378743.1(CYLD):c.2686+201_2686+202dup rs397717971
NM_001378743.1(CYLD):c.2686+202dup rs397717971
NM_001378743.1(CYLD):c.807+98_807+111del rs11271535
NM_001378743.1(CYLD):c.808-8A>G rs1555505165
NM_001378743.1(CYLD):c.923-188C>G rs73584473

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