ClinVar Miner

List of variants in gene PCDH15 reported as benign

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Gene type:
ClinVar version:
Total variants: 99
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HGVS dbSNP
GRCh37/hg19 10q21.1(chr10:55559110-55582905)x1
GRCh37/hg19 10q21.1(chr10:55943184-55991753)x3
GRCh37/hg19 10q21.1(chr10:56047470-56170113)x3
GRCh37/hg19 10q21.1(chr10:56233117-56288866)x3
GRCh37/hg19 10q21.1(chr10:56286068-56288866)x1
GRCh37/hg19 10q21.1(chr10:56423968-56469288)x3
GRCh37/hg19 10q21.1(chr10:56441012-56467563)x3
GRCh37/hg19 10q21.1(chr10:56452411-56480111)x3
GRCh37/hg19 10q21.1(chr10:56523671-56573906)x3
GRCh38/hg38 10q21.1(chr10:54417212-54436627)x3
GRCh38/hg38 10q21.1(chr10:55172554-55427295)x1
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.4501_4503delGAA (p.Glu1501del) rs561144747
NM_001142769.2(PCDH15):c.4562A>C (p.Glu1521Ala) rs149208928
NM_001142769.2(PCDH15):c.4596C>T (p.Ile1532=) rs12359240
NM_001142769.2(PCDH15):c.4623A>C (p.Thr1541=) rs16937769
NM_001142769.2(PCDH15):c.4853A>C (p.Glu1618Ala) rs11003863
NM_001142769.2(PCDH15):c.4853_4854delAGinsCC (p.Glu1618Ala) rs1554815737
NM_001142769.2(PCDH15):c.4854G>C (p.Glu1618Asp) rs531574437
NM_001142769.2(PCDH15):c.4947A>C (p.Glu1649Asp) rs16937768
NM_001142769.2(PCDH15):c.5236G>A (p.Gly1746Ser) rs7090408
NM_001142769.2(PCDH15):c.5295A>G (p.Pro1765=) rs145178582
NM_001142769.2(PCDH15):c.5298G>A (p.Ala1766=) rs139441645
NM_001142770.2(PCDH15):c.4522G>A (p.Val1508Met) rs41274622
NM_001142771.1(PCDH15):c.3389-4C>T rs111739360
NM_001142771.1(PCDH15):c.4554_4556dupAAC (p.Thr1519_Gly1520insThr) rs143978284
NM_001142771.1(PCDH15):c.4686G>A (p.Thr1562=) rs148772706
NM_001142771.1(PCDH15):c.4717C>T (p.Leu1573=) rs200155519
NM_001142771.1(PCDH15):c.4950G>A (p.Lys1650=) rs74609306
NM_001142771.1(PCDH15):c.4982A>C (p.Gln1661Pro) rs17704703
NM_033056.3(PCDH15):c.*12348A>G rs201855435
NM_033056.3(PCDH15):c.*12411C>T rs145418788
NM_033056.3(PCDH15):c.*9048G>A rs869312036
NM_033056.3(PCDH15):c.-5A>G rs142016527
NM_033056.3(PCDH15):c.1039C>T (p.Leu347Phe) rs111033436
NM_033056.3(PCDH15):c.1181A>G (p.Tyr394Cys) rs148533341
NM_033056.3(PCDH15):c.1304A>C (p.Asp435Ala) rs4935502
NM_033056.3(PCDH15):c.1306-4123C>T rs16905686
NM_033056.3(PCDH15):c.1360G>A (p.Val454Ile) rs61735473
NM_033056.3(PCDH15):c.1362C>T (p.Val454=) rs61735479
NM_033056.3(PCDH15):c.157+59097T>C rs75443986
NM_033056.3(PCDH15):c.1590+15_1590+19delAATAT rs202125339
NM_033056.3(PCDH15):c.1590+20A= rs7093302
NM_033056.3(PCDH15):c.1590+20A>G rs7093302
NM_033056.3(PCDH15):c.1702G>A (p.Ala568Thr) rs61730754
NM_033056.3(PCDH15):c.1910A>G (p.Asn637Ser) rs61731389
NM_033056.3(PCDH15):c.1917+33_1917+34delGT rs5785040
NM_033056.3(PCDH15):c.1917+33_1917+34dupGT rs5785040
NM_033056.3(PCDH15):c.2435T>C (p.Ile812Thr) rs61731363
NM_033056.3(PCDH15):c.2625G>A (p.Ser875=) rs111033516
NM_033056.3(PCDH15):c.2751+37C>T rs3812658
NM_033056.3(PCDH15):c.2751+43C>G rs2660169
NM_033056.3(PCDH15):c.2786G>A (p.Arg929Gln) rs2135720
NM_033056.3(PCDH15):c.2884C>T (p.Arg962Cys) rs201816080
NM_033056.3(PCDH15):c.2885G>A (p.Arg962His) rs45483395
NM_033056.3(PCDH15):c.3010-48G>A rs2593107
NM_033056.3(PCDH15):c.3018G>T (p.Val1006=) rs41307518
NM_033056.3(PCDH15):c.319-31T>C rs11594958
NM_033056.3(PCDH15):c.343G>A (p.Val115Met) rs143570915
NM_033056.3(PCDH15):c.3451G>A (p.Gly1151Arg) rs149478475
NM_033056.3(PCDH15):c.3502-14delT rs5785023
NM_033056.3(PCDH15):c.3502-14dup rs5785023
NM_033056.3(PCDH15):c.3502-8C>T rs184144118
NM_033056.3(PCDH15):c.3532G>A (p.Val1178Ile) rs147835286
NM_033056.3(PCDH15):c.3717+8G>C rs200556301
NM_033056.3(PCDH15):c.3718-19C>A rs75248212
NM_033056.3(PCDH15):c.3724G>A (p.Val1242Met) rs201137087
NM_033056.3(PCDH15):c.3795A>T (p.Glu1265Asp) rs111033496
NM_033056.3(PCDH15):c.3983+12T>C rs149867749
NM_033056.3(PCDH15):c.3984-20C>T rs7089209
NM_033056.3(PCDH15):c.4024C>A (p.Gln1342Lys) rs61731387
NM_033056.3(PCDH15):c.4334C>G (p.Ala1445Gly) rs146745502
NM_033056.3(PCDH15):c.4368-13_4368-10dupCTTT rs530804327
NM_033056.3(PCDH15):c.4581C>A (p.Pro1527=) rs10825114
NM_033056.3(PCDH15):c.475-3C>T rs41304641
NM_033056.3(PCDH15):c.4812G>T (p.Arg1604Ser) rs148718874
NM_033056.3(PCDH15):c.4831_4834dupAACA (p.Thr1612Lysfs) rs545191822
NM_033056.3(PCDH15):c.4884T>C (p.Thr1628=) rs16937781
NM_033056.3(PCDH15):c.5269_5277delTCTCCTCCT (p.Ser1757_Pro1759del) rs727503363
NM_033056.3(PCDH15):c.5286T>A (p.Pro1762=) rs58461416
NM_033056.3(PCDH15):c.5294_5302delTTGCTCCTC (p.Leu1765_Pro1767del) rs557936064
NM_033056.3(PCDH15):c.5359C>T (p.Pro1787Ser) rs61862390
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.5435C>T (p.Pro1812Leu) rs139668636
NM_033056.3(PCDH15):c.546A>G (p.Gly182=) rs34164469
NM_033056.3(PCDH15):c.5550C>A (p.Thr1850=) rs112097891
NM_033056.3(PCDH15):c.55T>G (p.Ser19Ala) rs11004439
NM_033056.3(PCDH15):c.5601_5603delAAC (p.Thr1869del) rs113363047
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= rs10740579
NM_033056.3(PCDH15):c.706-8C>T rs10740579
NM_033056.3(PCDH15):c.877-29G>T rs116339167
NM_033056.3(PCDH15):c.960A>G (p.Pro320=) rs41274634
NM_033056.3:c.+15180G>A
NM_033056.3:c.+15212A>C

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