List of variants in gene CDON 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: 26

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HGVS	dbSNP	gnomAD frequency
NM_001378964.1(CDON):c.3559C>T (p.Arg1187Cys)	rs150174788	0.00647
NM_001378964.1(CDON):c.2462G>A (p.Arg821His)	rs146660717	0.00102
NM_001378964.1(CDON):c.726G>A (p.Glu242=)	rs142667570	0.00040
NM_001378964.1(CDON):c.3631+9G>A	rs189386496	0.00039
NM_001378964.1(CDON):c.1041C>T (p.His347=)	rs201963480	0.00031
NM_001378964.1(CDON):c.1089C>T (p.Asn363=)	rs141744145	0.00028
NM_001378964.1(CDON):c.3706G>A (p.Glu1236Lys)	rs373765094	0.00021
NM_001378964.1(CDON):c.1025A>G (p.Asn342Ser)	rs140975280	0.00020
NM_001378964.1(CDON):c.2432G>A (p.Arg811His)	rs200008378	0.00016
NM_001378964.1(CDON):c.3099C>T (p.His1033=)	rs202230295	0.00014
NM_001378964.1(CDON):c.3120C>T (p.Gly1040=)	rs200405251	0.00014
NM_001378964.1(CDON):c.1414C>G (p.Pro472Ala)	rs750020763	0.00009
NM_001378964.1(CDON):c.3191G>A (p.Ser1064Asn)	rs113558382	0.00009
NM_001378964.1(CDON):c.2859G>T (p.Gly953=)	rs139149075	0.00004
NM_001378964.1(CDON):c.2159-8G>A	rs759480175	0.00003
NM_001378964.1(CDON):c.1553-17TC[6]
NM_001378964.1(CDON):c.1710C>T (p.Asn570=)
NM_001378964.1(CDON):c.1782C>T (p.Tyr594=)
NM_001378964.1(CDON):c.1824C>A (p.Ile608=)
NM_001378964.1(CDON):c.2211C>T (p.Val737=)
NM_001378964.1(CDON):c.2363-37GTT[3]	rs138741332
NM_001378964.1(CDON):c.244C>T (p.Leu82=)	rs552008016
NM_001378964.1(CDON):c.2685G>A (p.Gln895=)
NM_001378964.1(CDON):c.2996-31C>T
NM_001378964.1(CDON):c.3027A>T (p.Gly1009=)
NM_001378964.1(CDON):c.531G>A (p.Gln177=)

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