ClinVar Miner

List of variants in gene PKD1 reported as likely benign for not provided

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Total variants: 26
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HGVS dbSNP
NM_001009944.3(PKD1):c.10304G>A (p.Arg3435Gln) rs140189010
NM_001009944.3(PKD1):c.10325C>T (p.Ala3442Val) rs144593342
NM_001009944.3(PKD1):c.1123C>A (p.Leu375Ile)
NM_001009944.3(PKD1):c.11717G>T (p.Cys3906Phe) rs369291413
NM_001009944.3(PKD1):c.12237C>T (p.Ser4079=) rs372534935
NM_001009944.3(PKD1):c.12826C>T (p.Arg4276Trp) rs114251396
NM_001009944.3(PKD1):c.1304A>G (p.Gln435Arg) rs1426435123
NM_001009944.3(PKD1):c.1515C>T (p.Ala505=) rs748123570
NM_001009944.3(PKD1):c.1890G>A (p.Pro630=) rs1344519371
NM_001009944.3(PKD1):c.2643C>T (p.Phe881=)
NM_001009944.3(PKD1):c.3316C>G (p.Leu1106Val) rs141625744
NM_001009944.3(PKD1):c.4856C>T (p.Ser1619Phe) rs146723506
NM_001009944.3(PKD1):c.4917C>T (p.Gly1639=) rs148852027
NM_001009944.3(PKD1):c.5770G>A (p.Gly1924Ser) rs199947459
NM_001009944.3(PKD1):c.6792A>C (p.Ser2264=) rs142928249
NM_001009944.3(PKD1):c.6979C>T (p.Arg2327Trp) rs184394342
NM_001009944.3(PKD1):c.7280C>T (p.Ala2427Val) rs140494005
NM_001009944.3(PKD1):c.739C>T (p.Leu247Phe) rs537409943
NM_001009944.3(PKD1):c.7575C>T (p.Phe2525=) rs144409293
NM_001009944.3(PKD1):c.7605C>T (p.Tyr2535=)
NM_001009944.3(PKD1):c.8046G>A (p.Ser2682=)
NM_001009944.3(PKD1):c.8195G>A (p.Arg2732Gln) rs78185588
NM_001009944.3(PKD1):c.8751G>A (p.Ala2917=) rs746333408
NM_001009944.3(PKD1):c.9499A>T (p.Ile3167Phe) rs139945204
NM_001009944.3(PKD1):c.9582C>T (p.Ala3194=) rs1399957695
NM_001009944.3(PKD1):c.9829C>T (p.Arg3277Cys) rs148812376

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