List of variants in gene INPP5E 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_019892.6(INPP5E):c.1299G>A (p.Ala433=)	rs56931633	0.00272
NM_019892.6(INPP5E):c.1506G>A (p.Pro502=)	rs74880446	0.00100
NM_019892.6(INPP5E):c.1623C>T (p.Asp541=)	rs77248046	0.00068
NM_019892.6(INPP5E):c.469G>T (p.Gly157Trp)	rs78211353	0.00057
NM_019892.6(INPP5E):c.1191C>T (p.Ile397=)	rs558778286	0.00029
NM_019892.6(INPP5E):c.1176G>A (p.Thr392=)	rs528176529	0.00009
NM_019892.6(INPP5E):c.906C>T (p.Phe302=)	rs140222295	0.00006
NM_019892.6(INPP5E):c.1530C>T (p.Leu510=)	rs780119172	0.00001
NM_019892.6(INPP5E):c.957C>T (p.Asp319=)	rs1032007993	0.00001
NM_019892.6(INPP5E):c.1837C>T (p.Leu613=)
NM_019892.6(INPP5E):c.624A>G (p.Thr208=)

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