ClinVar Miner

List of variants in gene PCDH15 reported as likely benign

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Gene type:
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Total variants: 103
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HGVS dbSNP
NM_001142763.1(PCDH15):c.1153G>A (p.Gly385Ser) rs10825269
NM_001142763.1(PCDH15):c.1278T>C (p.Thr426=) rs7921598
NM_001142763.1(PCDH15):c.4871A>G (p.Asn1624Ser) rs111033362
NM_001142769.2(PCDH15):c.4575_4577delGGA (p.Glu1527del) rs1554815871
NM_001142769.2(PCDH15):c.5151T>C (p.Pro1717=) rs182175548
NM_001142769.2(PCDH15):c.5349T>C (p.Ser1783=) rs572152722
NM_001142771.1(PCDH15):c.4584G>A (p.Gln1528=) rs368096085
NM_001142771.1(PCDH15):c.4627G>A (p.Gly1543Ser) rs181306086
NM_001142771.1(PCDH15):c.4686G>A (p.Thr1562=) rs148772706
NM_033056.3(PCDH15):c.*12411C>T rs145418788
NM_033056.3(PCDH15):c.*414G>C rs16937780
NM_033056.3(PCDH15):c.1028G>A (p.Arg343Lys) rs141169746
NM_033056.3(PCDH15):c.1256A>G (p.Asn419Ser) rs143827620
NM_033056.3(PCDH15):c.1304A>C (p.Asp435Ala) rs4935502
NM_033056.3(PCDH15):c.1362C>T (p.Val454=) rs61735479
NM_033056.3(PCDH15):c.158-16930T>C rs207470941
NM_033056.3(PCDH15):c.1653G>A (p.Gly551=) rs141281651
NM_033056.3(PCDH15):c.1702G>A (p.Ala568Thr) rs61730754
NM_033056.3(PCDH15):c.1784+11T>G rs769008985
NM_033056.3(PCDH15):c.195T>C (p.Thr65=) rs770371293
NM_033056.3(PCDH15):c.1998-13G>A rs727504616
NM_033056.3(PCDH15):c.2092-6T>C rs780684363
NM_033056.3(PCDH15):c.2379T>C (p.Asp793=) rs148920891
NM_033056.3(PCDH15):c.2385A>G (p.Ala795=) rs61731362
NM_033056.3(PCDH15):c.2424G>C (p.Lys808Asn) rs375855445
NM_033056.3(PCDH15):c.2435T>C (p.Ile812Thr) rs61731363
NM_033056.3(PCDH15):c.243G>A (p.Val81=) rs151119732
NM_033056.3(PCDH15):c.2538C>T (p.Val846=) rs727504573
NM_033056.3(PCDH15):c.2563C>T (p.Arg855Trp) rs138010738
NM_033056.3(PCDH15):c.2625G>A (p.Ser875=) rs111033516
NM_033056.3(PCDH15):c.2721T>G (p.Pro907=) rs727504835
NM_033056.3(PCDH15):c.2769T>C (p.Pro923=) rs727503366
NM_033056.3(PCDH15):c.2786G>A (p.Arg929Gln) rs2135720
NM_033056.3(PCDH15):c.2811G>A (p.Pro937=) rs1449039709
NM_033056.3(PCDH15):c.2859A>C (p.Ala953=) rs375965861
NM_033056.3(PCDH15):c.2885G>T (p.Arg962Leu) rs45483395
NM_033056.3(PCDH15):c.2990A>G (p.Glu997Gly) rs139087859
NM_033056.3(PCDH15):c.3195A>G (p.Gln1065=) rs776720353
NM_033056.3(PCDH15):c.3276T>C (p.Asn1092=) rs772160626
NM_033056.3(PCDH15):c.330C>T (p.Asn110=) rs146796009
NM_033056.3(PCDH15):c.3327T>C (p.Ala1109=) rs1554871942
NM_033056.3(PCDH15):c.3374-16G>A rs139684809
NM_033056.3(PCDH15):c.343G>A (p.Val115Met) rs143570915
NM_033056.3(PCDH15):c.3444C>T (p.Phe1148=) rs876657562
NM_033056.3(PCDH15):c.3451G>A (p.Gly1151Arg) rs149478475
NM_033056.3(PCDH15):c.3498G>A (p.Val1166=) rs1554852336
NM_033056.3(PCDH15):c.3501+13A>G rs727503365
NM_033056.3(PCDH15):c.3502-8C>T rs184144118
NM_033056.3(PCDH15):c.3532G>A (p.Val1178Ile) rs147835286
NM_033056.3(PCDH15):c.3585T>C (p.Phe1195=) rs397517457
NM_033056.3(PCDH15):c.369A>G (p.Lys123=) rs1317246200
NM_033056.3(PCDH15):c.3717+8G>C rs200556301
NM_033056.3(PCDH15):c.3877C>A (p.Arg1293=) rs142034111
NM_033056.3(PCDH15):c.3936A>G (p.Ala1312=) rs398124433
NM_033056.3(PCDH15):c.4024C>A (p.Gln1342Lys) rs61731387
NM_033056.3(PCDH15):c.4080G>A (p.Val1360=) rs111033499
NM_033056.3(PCDH15):c.4103A>G (p.Glu1368Gly) rs111033449
NM_033056.3(PCDH15):c.4314G>A (p.Pro1438=) rs535913178
NM_033056.3(PCDH15):c.4317G>A (p.Pro1439=) rs370470900
NM_033056.3(PCDH15):c.4367+8G>A rs727504745
NM_033056.3(PCDH15):c.4368-76C>T rs375657329
NM_033056.3(PCDH15):c.4368-77G>A rs776152870
NM_033056.3(PCDH15):c.4368-77delG rs1554821197
NM_033056.3(PCDH15):c.4368-79_4368-76delGAGC rs1554821194
NM_033056.3(PCDH15):c.4463A>G (p.Asn1488Ser) rs201534861
NM_033056.3(PCDH15):c.4568G>A (p.Ser1523Asn) rs1377421029
NM_033056.3(PCDH15):c.4581C>A (p.Pro1527=) rs10825114
NM_033056.3(PCDH15):c.4677G>A (p.Lys1559=) rs375077719
NM_033056.3(PCDH15):c.4733T>C (p.Val1578Ala) rs139915181
NM_033056.3(PCDH15):c.4783A>C (p.Ile1595Leu) rs397517461
NM_033056.3(PCDH15):c.4788T>G (p.Asp1596Glu) rs200659780
NM_033056.3(PCDH15):c.4837G>A (p.Gly1613Arg) rs876657563
NM_033056.3(PCDH15):c.4884T>C (p.Thr1628=) rs16937781
NM_033056.3(PCDH15):c.4974A>C (p.Ser1658=) rs147993163
NM_033056.3(PCDH15):c.5189T>A (p.Ile1730Asn) rs727503364
NM_033056.3(PCDH15):c.5254_5256delCCT (p.Pro1752del) rs397517462
NM_033056.3(PCDH15):c.5278_5286delCCTGCTCCT (p.Pro1760_Pro1762del) rs373916538
NM_033056.3(PCDH15):c.5280_5342del63 (p.Ala1761_Pro1781del) rs1554820012
NM_033056.3(PCDH15):c.5283T>A (p.Ala1761=) rs375134176
NM_033056.3(PCDH15):c.5286T>A (p.Pro1762=) rs58461416
NM_033056.3(PCDH15):c.5287_5292delGCTCCT (p.Ala1763_Pro1764del) rs397517465
NM_033056.3(PCDH15):c.5296_5304dupGCTCCTCCT (p.Pro1768_Pro1769insAlaProPro) rs397517466
NM_033056.3(PCDH15):c.5327_5335delTTTTTTGTC (p.Leu1776_Cys1778del) rs397517467
NM_033056.3(PCDH15):c.5334T>C (p.Cys1778=) rs727503362
NM_033056.3(PCDH15):c.5346T>A (p.Ser1782=) rs397517468
NM_033056.3(PCDH15):c.5349T>G (p.Pro1783=) rs727505113
NM_033056.3(PCDH15):c.5352T>A (p.Pro1784=) rs727505100
NM_033056.3(PCDH15):c.5353T>C (p.Ser1785Pro) rs144261647
NM_033056.3(PCDH15):c.5359C>T (p.Pro1787Ser) rs61862390
NM_033056.3(PCDH15):c.5397C>T (p.Ser1799=) rs367881384
NM_033056.3(PCDH15):c.5398G>A (p.Val1800Ile) rs111033463
NM_033056.3(PCDH15):c.5414C>T (p.Pro1805Leu) rs114137983
NM_033056.3(PCDH15):c.5424A>C (p.Pro1808=) rs753289924
NM_033056.3(PCDH15):c.5439A>C (p.Pro1813=) rs150303579
NM_033056.3(PCDH15):c.5550C>A (p.Thr1850=) rs112097891
NM_033056.3(PCDH15):c.5557A>C (p.Met1853Leu) rs145903555
NM_033056.3(PCDH15):c.5565C>T (p.Ala1855=) rs111033445
NM_033056.3(PCDH15):c.55T>G (p.Ser19Ala) rs11004439
NM_033056.3(PCDH15):c.5603C>T (p.Thr1868Met) rs191736346
NM_033056.3(PCDH15):c.5707A>G (p.Ile1903Val) rs79854148
NM_033056.3(PCDH15):c.706-8C>T rs10740579
NM_033056.3(PCDH15):c.913C>G (p.Gln305Glu) rs143058902
NM_033056.3(PCDH15):c.942A>G (p.Gln314=) rs149481989

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