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: 26
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HGVS dbSNP
NM_017882.3(CLN6):c.138C>T (p.Asp46=) rs1595821372
NM_017882.3(CLN6):c.199-70G>A rs114850355
NM_017882.3(CLN6):c.298-168C>T rs56883694
NM_017882.3(CLN6):c.298-6C>T rs117038427
NM_017882.3(CLN6):c.36G>A (p.Ala12=) rs1048000119
NM_017882.3(CLN6):c.441T>G (p.Ser147=) rs1595818241
NM_017882.3(CLN6):c.486+8C>T rs149692285
NM_017882.3(CLN6):c.487-39C>T rs116956347
NM_017882.3(CLN6):c.49G>A (p.Gly17Ser) rs763944821
NM_017882.3(CLN6):c.507C>T (p.Leu169=) rs1273285939
NM_017882.3(CLN6):c.516T>C (p.Tyr172=)
NM_017882.3(CLN6):c.522G>A (p.Glu174=) rs753538013
NM_017882.3(CLN6):c.542+212C>T rs111504155
NM_017882.3(CLN6):c.552C>T (p.Pro184=) rs1595817219
NM_017882.3(CLN6):c.555C>T (p.Phe185=) rs1595817218
NM_017882.3(CLN6):c.564C>T (p.Ile188=) rs371326037
NM_017882.3(CLN6):c.636C>T (p.Leu212=) rs758612277
NM_017882.3(CLN6):c.678C>T (p.Thr226=) rs374744816
NM_017882.3(CLN6):c.684C>A (p.Gly228=) rs1209133488
NM_017882.3(CLN6):c.759C>G (p.Leu253=) rs1567094628
NM_017882.3(CLN6):c.763C>T (p.Leu255=) rs1195840845
NM_017882.3(CLN6):c.769A>G (p.Ser257Gly) rs151295143
NM_017882.3(CLN6):c.774C>T (p.Asn258=) rs1555438231
NM_017882.3(CLN6):c.83+7G>A rs1595826955
NM_017882.3(CLN6):c.84-81C>T rs117298614
NM_017882.3(CLN6):c.84-9C>T rs778471506

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