List of variants in gene CNN1

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_001299.6(CNN1):c.15C>G (p.His5Gln)	rs150521786	0.00044
NM_001299.6(CNN1):c.727G>A (p.Val243Ile)	rs369315192	0.00013
NM_001299.6(CNN1):c.553C>T (p.Arg185Trp)	rs201786372	0.00011
NM_001299.6(CNN1):c.539C>T (p.Thr180Met)	rs146897323	0.00009
NM_001299.6(CNN1):c.88C>T (p.Arg30Trp)	rs149734482	0.00009
NM_001299.6(CNN1):c.410A>T (p.Lys137Met)	rs199856281	0.00005
NM_001299.6(CNN1):c.803A>G (p.Tyr268Cys)	rs765580270	0.00004
NM_001299.6(CNN1):c.556C>T (p.Arg186Cys)	rs368198606	0.00002
NM_001299.6(CNN1):c.310G>A (p.Asp104Asn)	rs375046434	0.00001
NM_001299.6(CNN1):c.313A>G (p.Ile105Val)	rs774820435	0.00001
NM_001299.6(CNN1):c.516G>C (p.Lys172Asn)	rs748546504	0.00001
NM_001299.6(CNN1):c.554G>A (p.Arg185Gln)	rs776419314	0.00001
NM_001299.6(CNN1):c.734T>A (p.Leu245Gln)	rs1972673215	0.00001
NM_001299.6(CNN1):c.880T>C (p.Tyr294His)	rs1429198242	0.00001
NM_001299.6(CNN1):c.127G>A (p.Gly43Ser)
NM_001299.6(CNN1):c.157G>T (p.Gly53Cys)	rs759065611
NM_001299.6(CNN1):c.311A>T (p.Asp104Val)	rs2512688229
NM_001299.6(CNN1):c.461C>A (p.Pro154Gln)	rs117853664
NM_001299.6(CNN1):c.473G>A (p.Arg158Lys)
NM_001299.6(CNN1):c.487A>G (p.Ile163Val)
NM_001299.6(CNN1):c.49G>A (p.Glu17Lys)
NM_001299.6(CNN1):c.509C>A (p.Thr170Asn)	rs1169442174
NM_001299.6(CNN1):c.564C>T (p.Leu188=)	rs147229692
NM_001299.6(CNN1):c.725A>G (p.Asn242Ser)	rs148602672
NM_001299.6(CNN1):c.770G>A (p.Gly257Asp)	rs866050250
NM_001299.6(CNN1):c.865C>G (p.His289Asp)	rs756852254
NM_001299.6(CNN1):c.869C>T (p.Ala290Val)
NM_001299.6(CNN1):c.89G>A (p.Arg30Gln)	rs201339097

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