ClinVar Miner

List of variants in gene CLN6 reported as likely benign for not provided

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Gene type:
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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_017882.3(CLN6):c.297+158C>T rs11638475 0.02178
NC_000015.10:g.68229762A>G rs375902554 0.01863
NM_017882.3(CLN6):c.298-168C>T rs56883694 0.01346
NM_017882.3(CLN6):c.486+8C>T rs149692285 0.01339
NM_017882.3(CLN6):c.542+165C>T rs17317039 0.01189
NM_017882.3(CLN6):c.543-303G>A rs148243823 0.01154
NM_017882.3(CLN6):c.34G>A (p.Ala12Thr) rs112239768 0.01081
NM_017882.3(CLN6):c.542+212C>T rs111504155 0.00812
NM_017882.3(CLN6):c.*30T>G rs758756489 0.00700
NM_017882.3(CLN6):c.84-81C>T rs117298614 0.00698
NM_017882.3(CLN6):c.199-84C>T rs7182333 0.00619
NM_017882.3(CLN6):c.*646C>G rs144976448 0.00573
NM_017882.3(CLN6):c.298-6C>T rs117038427 0.00549
NM_017882.3(CLN6):c.487-39C>T rs116956347 0.00549
NM_017882.3(CLN6):c.*393G>A rs114833125 0.00546
NM_017882.3(CLN6):c.83+218G>T rs541105748 0.00509
NM_017882.3(CLN6):c.199-70G>A rs114850355 0.00479
NM_017882.3(CLN6):c.769A>G (p.Ser257Gly) rs151295143 0.00475
NM_017882.3(CLN6):c.487-140G>A rs74020079 0.00436
NM_017882.3(CLN6):c.*75G>C rs57058289 0.00367
NM_017882.3(CLN6):c.542+33G>A rs548821903 0.00342
NM_017882.3(CLN6):c.840G>A (p.Leu280=) rs148949069 0.00198
NM_017882.3(CLN6):c.923G>C (p.Ser308Thr) rs143578698 0.00169
NM_017882.3(CLN6):c.214G>C (p.Glu72Gln) rs104894483 0.00140
NM_017882.3(CLN6):c.822G>A (p.Ala274=) rs151186473 0.00041
NM_017882.3(CLN6):c.42C>A (p.Gly14=) rs373776911 0.00036
NM_017882.3(CLN6):c.-23G>A rs536088577 0.00028
NM_017882.3(CLN6):c.84-18C>T rs201554701 0.00022
NM_017882.3(CLN6):c.741C>T (p.His247=) rs140653271 0.00020
NM_017882.3(CLN6):c.477G>A (p.Pro159=) rs370811678 0.00013
NM_017882.3(CLN6):c.199-5C>T rs371705916 0.00006
NM_017882.3(CLN6):c.666-45C>T rs201306069 0.00006
NM_017882.3(CLN6):c.799G>A (p.Ala267Thr) rs374613712 0.00006
NM_017882.3(CLN6):c.678C>T (p.Thr226=) rs374744816 0.00005
NM_017882.3(CLN6):c.72C>T (p.Phe24=) rs767394326 0.00005
NM_017882.3(CLN6):c.103G>A (p.Asp35Asn) rs533231370 0.00004
NM_017882.3(CLN6):c.49G>A (p.Gly17Ser) rs763944821 0.00002
NM_017882.3(CLN6):c.582C>T (p.Ser194=) rs769007090 0.00002
NM_017882.3(CLN6):c.516T>C (p.Tyr172=) rs547002745 0.00001
NM_001411068.1(CLN6):c.46C>T (p.Arg16Trp)
NM_017882.3(CLN6):c.*141GT[12] rs3837692
NM_017882.3(CLN6):c.*141GT[14] rs3837692
NM_017882.3(CLN6):c.*141GT[9] rs3837692
NM_017882.3(CLN6):c.54G>A (p.Ala18=) rs1199248099
NM_017882.3(CLN6):c.64G>T (p.Ala22Ser) rs527373013
NM_017882.3(CLN6):c.684C>A (p.Gly228=) rs1209133488
NM_017882.3(CLN6):c.789C>T (p.Phe263=)
NM_017882.3(CLN6):c.83+188_83+191del rs66812362
NM_017882.3(CLN6):c.83+225del rs577777835
NM_017882.3(CLN6):c.876T>C (p.Gly292=) rs916275768

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