List of variants in gene combination CFTR, LOC111674472 reported by Revvity Omics, Revvity

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000492.4(CFTR):c.2991G>C (p.Leu997Phe)	rs1800111	0.00208
NM_000492.4(CFTR):c.3209G>A (p.Arg1070Gln)	rs78769542	0.00030
NM_000492.4(CFTR):c.3200C>T (p.Ala1067Val)	rs1800114	0.00005
NM_000492.4(CFTR):c.3169A>G (p.Thr1057Ala)	rs397508511	0.00004
NM_000492.4(CFTR):c.3038C>A (p.Pro1013His)	rs193922516	0.00003
NM_000492.4(CFTR):c.3275A>G (p.Tyr1092Cys)	rs764434414	0.00001
NM_000492.4(CFTR):c.2989-1G>A	rs397508470
NM_000492.4(CFTR):c.3067_3072del (p.Ile1023_Val1024del)	rs121908767
NM_000492.4(CFTR):c.3353C>T (p.Ser1118Phe)	rs146521846

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