List of variants in gene CDC42BPG reported as likely benign by Ambry Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_017525.3(CDC42BPG):c.1706C>T (p.Thr569Met)	rs149415030	0.00023
NM_017525.3(CDC42BPG):c.1463G>A (p.Arg488Gln)	rs141461205	0.00021
NM_017525.3(CDC42BPG):c.1928G>A (p.Arg643Gln)	rs201215892	0.00008
NM_017525.3(CDC42BPG):c.1940G>A (p.Arg647Gln)	rs202075477	0.00006
NM_017525.3(CDC42BPG):c.3359G>A (p.Arg1120His)	rs769794565	0.00005
NM_017525.3(CDC42BPG):c.1250G>A (p.Arg417Gln)	rs1396542698	0.00003
NM_017525.3(CDC42BPG):c.2374G>A (p.Ala792Thr)	rs763474884	0.00001
NM_017525.3(CDC42BPG):c.2804G>A (p.Arg935His)	rs775011367	0.00001
NM_017525.3(CDC42BPG):c.1487G>A (p.Arg496Gln)
NM_017525.3(CDC42BPG):c.1622G>A (p.Arg541Gln)	rs771569916
NM_017525.3(CDC42BPG):c.1697G>A (p.Arg566Gln)	rs542288032
NM_017525.3(CDC42BPG):c.2582C>T (p.Ala861Val)
NM_017525.3(CDC42BPG):c.4388C>G (p.Pro1463Arg)

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