List of variants reported as likely pathogenic for Ectopic tissue by Genetic Services Laboratory, University of Chicago

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Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_001195553.2(DCX):c.167G>C (p.Arg56Pro)	rs587783525
NM_001195553.2(DCX):c.170T>G (p.Phe57Cys)	rs587783526
NM_001195553.2(DCX):c.185A>G (p.Asp62Gly)	rs587783528
NM_001195553.2(DCX):c.187C>T (p.Arg63Cys)	rs587783529
NM_001195553.2(DCX):c.191A>G (p.Tyr64Cys)	rs587783530
NM_001195553.2(DCX):c.195C>A (p.Phe65Leu)	rs587783531
NM_001195553.2(DCX):c.226C>T (p.Arg76Cys)	rs587783534
NM_001195553.2(DCX):c.299G>A (p.Gly100Glu)	rs587783538
NM_001195553.2(DCX):c.337A>T (p.Ile113Phe)	rs587783542
NM_001195553.2(DCX):c.377T>A (p.Val126Asp)	rs587783546
NM_001195553.2(DCX):c.380G>A (p.Cys127Tyr)	rs587783547
NM_001195553.2(DCX):c.551T>A (p.Ile184Asn)	rs587783561
NM_001195553.2(DCX):c.571C>A (p.Pro191Thr)	rs587783565
NM_001195553.2(DCX):c.596T>C (p.Leu199Pro)	rs587783569
NM_001195553.2(DCX):c.614A>T (p.His205Leu)	rs587783572
NM_001195553.2(DCX):c.688A>C (p.Thr230Pro)	rs587783581
NM_001195553.2(DCX):c.724T>A (p.Phe242Ile)	rs587783582
NM_001195553.2(DCX):c.746T>G (p.Phe249Cys)	rs587783584
NM_001195553.2(DCX):c.773G>C (p.Arg258Pro)	rs587783587

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