List of variants in gene PPP2R5D reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_006245.4(PPP2R5D):c.1284T>C (p.Asn428=)	rs114970216	0.00555
NM_006245.4(PPP2R5D):c.1558C>T (p.Pro520Ser)	rs139183911	0.00050
NM_006245.4(PPP2R5D):c.1614C>T (p.Thr538=)	rs150410961	0.00027
NM_006245.4(PPP2R5D):c.885C>T (p.Asn295=)	rs768102492	0.00024
NM_006245.4(PPP2R5D):c.188C>T (p.Thr63Met)	rs370244516	0.00003
NM_006245.4(PPP2R5D):c.1322G>A (p.Arg441Gln)	rs748607156	0.00002
NM_006245.4(PPP2R5D):c.1092A>G (p.Gly364=)
NM_006245.4(PPP2R5D):c.1401T>C (p.Tyr467=)
NM_006245.4(PPP2R5D):c.1419T>C (p.Phe473=)
NM_006245.4(PPP2R5D):c.1598C>T (p.Ser533Leu)
NM_006245.4(PPP2R5D):c.198C>T (p.Pro66=)	rs146145609
NM_006245.4(PPP2R5D):c.322+4C>A	rs1031636348
NM_006245.4(PPP2R5D):c.36C>A (p.Pro12=)
NM_006245.4(PPP2R5D):c.687C>T (p.Asn229=)

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