List of variants in gene combination CDK4, TSPAN31 reported as uncertain significance by GeneDx

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_000075.4(CDK4):c.779T>A (p.Val260Glu)	rs200215596	0.00013
NM_000075.4(CDK4):c.886C>T (p.His296Tyr)	rs2227954	0.00008
NM_000075.4(CDK4):c.776C>T (p.Ser259Leu)	rs201617914	0.00007
NM_000075.4(CDK4):c.863G>A (p.Arg288Gln)	rs761577371	0.00004
NM_000075.4(CDK4):c.898G>A (p.Gly300Ser)	rs879254241	0.00004
NM_000075.4(CDK4):c.736C>T (p.Arg246Cys)	rs370258992	0.00003
NM_000075.4(CDK4):c.661G>A (p.Asp221Asn)	rs587778187	0.00002
NM_000075.4(CDK4):c.806C>T (p.Ala269Val)	rs779161525	0.00002
NM_000075.4(CDK4):c.869T>C (p.Leu290Pro)	rs768127244	0.00002
NM_000075.4(CDK4):c.689T>C (p.Ile230Thr)	rs760435132	0.00001
NM_000075.4(CDK4):c.700C>T (p.Pro234Ser)	rs1474793589	0.00001
NM_000075.4(CDK4):c.719G>A (p.Arg240Gln)	rs531817742	0.00001
NM_000075.4(CDK4):c.778G>T (p.Val260Leu)	rs876660340	0.00001
NM_000075.4(CDK4):c.800C>T (p.Ser267Leu)	rs1157646541	0.00001
NM_000075.4(CDK4):c.829A>G (p.Thr277Ala)	rs767343306	0.00001
NM_000075.4(CDK4):c.892G>A (p.Asp298Asn)	rs1367425262	0.00001
NM_000075.4(CDK4):c.684C>G (p.Asp228Glu)
NM_000075.4(CDK4):c.724G>A (p.Val242Ile)	rs876658903
NM_000075.4(CDK4):c.757G>C (p.Gly253Arg)	rs1955201304
NM_000075.4(CDK4):c.760C>T (p.Pro254Ser)	rs587779896
NM_000075.4(CDK4):c.823A>T (p.Met275Leu)	rs587781723
NM_000075.4(CDK4):c.833_834del (p.Thr277_Phe278insTer)
NM_000075.4(CDK4):c.850A>G (p.Ile284Val)	rs730881671
NM_000075.4(CDK4):c.862C>G (p.Arg288Gly)	rs587779897

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