List of variants in gene CFTR reported as benign for not specified

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: 49

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HGVS	dbSNP	gnomAD frequency
NM_000492.4(CFTR):c.1408G>A (p.Val470Met)	rs213950	0.56732
NM_000492.4(CFTR):c.1680-870T>A	rs213965	0.55332
NM_000492.4(CFTR):c.2562T>G (p.Thr854=)	rs1042077	0.44737
NM_000492.4(CFTR):c.1408= (p.Val470=)	rs213950	0.43268
NM_000492.4(CFTR):c.1767-136T>C	rs11978434	0.20764
NM_000492.4(CFTR):c.1210-13G>T	rs10229820	0.09791
NM_000492.4(CFTR):c.869+11C>T	rs1800503	0.07590
NM_000492.4(CFTR):c.3870A>G (p.Pro1290=)	rs1800130	0.07467
NM_000492.4(CFTR):c.743+40A>G	rs1800502	0.03675
NM_000492.4(CFTR):c.1584G>A (p.Glu528=)	rs1800095	0.01670
NM_000492.4(CFTR):c.*1043A>C	rs10234329	0.01452
NM_000492.4(CFTR):c.2898G>A (p.Thr966=)	rs1800109	0.00907
NM_000492.4(CFTR):c.164+28A>G	rs34010645	0.00589
NM_000492.4(CFTR):c.3705T>G (p.Ser1235Arg)	rs34911792	0.00573
NM_000492.4(CFTR):c.1581A>G (p.Glu527=)	rs1800094	0.00491
NM_000492.4(CFTR):c.4242+13A>G	rs76179227	0.00295
NM_000492.4(CFTR):c.1210-13del	rs750294275	0.00222
NM_000492.4(CFTR):c.2620-15C>G	rs139379077	0.00212
NM_000492.4(CFTR):c.1365G>A (p.Ala455=)	rs79074685	0.00183
NM_000492.4(CFTR):c.1393-42G>A	rs34906874	0.00148
NM_000492.4(CFTR):c.2820T>G (p.Thr940=)	rs60887846	0.00148
NM_000492.4(CFTR):c.853A>T (p.Ile285Phe)	rs151073129	0.00145
NM_000492.4(CFTR):c.91C>T (p.Arg31Cys)	rs1800073	0.00134
NM_000492.4(CFTR):c.4242+10T>C	rs138642693	0.00127
NM_000492.4(CFTR):c.3897A>G (p.Thr1299=)	rs1800131	0.00101
NM_000492.4(CFTR):c.1523T>G (p.Phe508Cys)	rs74571530	0.00090
NM_000492.4(CFTR):c.443T>C (p.Ile148Thr)	rs35516286	0.00083
NM_000492.4(CFTR):c.2735C>T (p.Ser912Leu)	rs121909034	0.00068
NM_000492.4(CFTR):c.3717+45G>A	rs145743767	0.00058
NM_000492.4(CFTR):c.3469-17T>C	rs199630678	0.00041
NM_000492.4(CFTR):c.2506G>T (p.Asp836Tyr)	rs201386642	0.00040
NM_000492.4(CFTR):c.1920T>C (p.Phe640=)	rs145877746	0.00036
NM_000492.4(CFTR):c.1516A>G (p.Ile506Val)	rs1800091	0.00034
NM_000492.4(CFTR):c.2604A>G (p.Val868=)	rs1800105	0.00006
NM_000492.4(CFTR):c.3469-20T>C	rs373002889	0.00005
NM_000492.3(CFTR):c.1210-12T[9]	rs1805177
NM_000492.3(CFTR):c.1210-17_1210-12del	rs3832534
NM_000492.4(CFTR):c.1210-14_1210-13insTG	rs796065326
NM_000492.4(CFTR):c.1210-34TG[10]	rs3832534
NM_000492.4(CFTR):c.1210-34TG[12]	rs3832534
NM_000492.4(CFTR):c.1251C>A (p.Asn417Lys)	rs4727853
NM_000492.4(CFTR):c.1254T>C (p.Asn418=)	rs62469440
NM_000492.4(CFTR):c.1584+53_1584+63dup	rs397508232
NM_000492.4(CFTR):c.224G>A (p.Arg75Gln)	rs1800076
NM_000492.4(CFTR):c.2684G>A (p.Ser895Asn)	rs201864483
NM_000492.4(CFTR):c.3485G>T (p.Arg1162Leu)	rs1800120
NM_000492.4(CFTR):c.54-589A>G
NM_000492.4(CFTR):c.744-33GATT[6]	rs1805171
NM_000492.4(CFTR):c.744-33GATT[8]	rs1805171

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