List of variants in gene PCDH15 reported as benign by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_001384140.1(PCDH15):c.706-8C>T	rs10740579	0.71606
NM_001384140.1(PCDH15):c.1138G>A (p.Gly380Ser)	rs10825269	0.22813
NM_001384140.1(PCDH15):c.4671+1344A>C	rs11003863	0.17427
NM_001384140.1(PCDH15):c.1304A>C (p.Asp435Ala)	rs4935502	0.15952
NM_033056.4(PCDH15):c.4581C>A (p.Pro1527=)	rs10825114	0.12444
NM_033056.4(PCDH15):c.5707A>G (p.Ile1903Val)	rs79854148	0.03803
NM_033056.4(PCDH15):c.5359C>T (p.Pro1787Ser)	rs61862390	0.01583
NM_001384140.1(PCDH15):c.1360G>A (p.Val454Ile)	rs61735473	0.00870
NM_001384140.1(PCDH15):c.4672-1637G>A	rs139441645	0.00746
NM_001384140.1(PCDH15):c.4024C>A (p.Gln1342Lys)	rs61731387	0.00699
NM_033056.4(PCDH15):c.4850A>G (p.Asn1617Ser)	rs111033362	0.00631
NM_001384140.1(PCDH15):c.4671+1087C>T	rs12359240	0.00438
NM_033056.4(PCDH15):c.5603C>T (p.Thr1868Met)	rs191736346	0.00423
NM_001384140.1(PCDH15):c.3502-8C>T	rs184144118	0.00411
NM_001384140.1(PCDH15):c.2435T>C (p.Ile812Thr)	rs61731363	0.00325
NM_001384140.1(PCDH15):c.1039C>T (p.Leu347Phe)	rs111033436	0.00318
NM_001384140.1(PCDH15):c.3717+8G>C	rs200556301	0.00305
NM_001384140.1(PCDH15):c.1362C>T (p.Val454=)	rs61735479	0.00267
NM_001384140.1(PCDH15):c.4672-1640A>G	rs145178582	0.00232
NM_033056.4(PCDH15):c.5286T>A (p.Pro1762=)	rs58461416	0.00220
NM_001384140.1(PCDH15):c.3018G>T (p.Val1006=)	rs41307518	0.00149
NM_001384140.1(PCDH15):c.2885G>A (p.Arg962His)	rs45483395
NM_001384140.1(PCDH15):c.4651GAA[1] (p.Glu1552del)	rs561144747
NM_033056.3(PCDH15):c.4368-13_4368-10dup	rs530804327
NM_033056.4(PCDH15):c.4831_4834dup (p.Thr1612fs)	rs545191822
NM_033056.4(PCDH15):c.5294_5302del (p.Leu1765_Pro1767del)	rs557936064
NM_033056.4(PCDH15):c.5598AAC[1] (p.Thr1869del)	rs113363047

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