List of variants in gene WDPCP reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 38

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HGVS	dbSNP	gnomAD frequency
NM_015910.7(WDPCP):c.499+20A>G	rs186575824	0.00159
NM_015910.7(WDPCP):c.176T>A (p.Ile59Asn)	rs202196322	0.00156
NM_015910.7(WDPCP):c.220G>C (p.Gly74Arg)	rs200170138	0.00042
NM_015910.7(WDPCP):c.826-8C>A	rs201860952	0.00040
NM_015910.7(WDPCP):c.252G>T (p.Glu84Asp)	rs201399904	0.00028
NM_015910.7(WDPCP):c.1788C>T (p.Asp596=)	rs185980830	0.00026
NM_015910.7(WDPCP):c.480C>T (p.Ile160=)	rs768777510	0.00024
NM_015910.7(WDPCP):c.1789G>A (p.Val597Ile)	rs776917693	0.00020
NM_015910.7(WDPCP):c.1079C>T (p.Ser360Leu)	rs141011629	0.00014
NM_015910.7(WDPCP):c.2113G>T (p.Asp705Tyr)	rs200378703	0.00014
NM_015910.7(WDPCP):c.1310G>T (p.Ser437Ile)	rs367727948	0.00012
NM_015910.7(WDPCP):c.868C>T (p.Arg290Cys)	rs374934704	0.00010
NM_015910.7(WDPCP):c.2178C>T (p.Asp726=)	rs367690400	0.00007
NM_015910.7(WDPCP):c.159G>A (p.Ala53=)	rs192196713	0.00004
NM_015910.7(WDPCP):c.2160C>T (p.Asp720=)	rs372727422	0.00004
NM_015910.7(WDPCP):c.276C>T (p.Leu92=)	rs759303585	0.00004
NM_015910.7(WDPCP):c.60C>A (p.Ser20=)	rs757553495	0.00004
NM_015910.7(WDPCP):c.915C>T (p.Ser305=)	rs370372057	0.00004
NM_015910.7(WDPCP):c.1575C>T (p.Ser525=)	rs375693256	0.00003
NM_015910.7(WDPCP):c.33C>T (p.Ser11=)	rs557213834	0.00003
NM_015910.7(WDPCP):c.1671A>G (p.Pro557=)	rs202162023	0.00002
NM_015910.7(WDPCP):c.1587C>T (p.Asn529=)	rs763698807	0.00001
NM_015910.7(WDPCP):c.255A>G (p.Ser85=)	rs1252079324	0.00001
NM_015910.7(WDPCP):c.30C>T (p.Tyr10=)	rs1248204391	0.00001
NM_015910.7(WDPCP):c.654C>T (p.Pro218=)	rs375737055	0.00001
NM_015910.7(WDPCP):c.1425G>A (p.Leu475=)
NM_015910.7(WDPCP):c.1695A>G (p.Glu565=)
NM_015910.7(WDPCP):c.1731C>T (p.Phe577=)	rs778132438
NM_015910.7(WDPCP):c.1748+18358G>A
NM_015910.7(WDPCP):c.1813-3C>T	rs772639117
NM_015910.7(WDPCP):c.2088T>C (p.Ile696=)
NM_015910.7(WDPCP):c.500-304C>T
NM_015910.7(WDPCP):c.500-321G>A
NM_015910.7(WDPCP):c.60C>T (p.Ser20=)
NM_015910.7(WDPCP):c.63A>G (p.Pro21=)
NM_015910.7(WDPCP):c.661A>G (p.Ile221Val)	rs571641878
NM_015910.7(WDPCP):c.76-15_76-5del	rs780314107
NM_015910.7(WDPCP):c.924A>G (p.Val308=)	rs201844706

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