List of variants in gene MUC5B reported as likely 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: 34

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HGVS	dbSNP	gnomAD frequency
NM_002458.3(MUC5B):c.15861A>G (p.Pro5287=)	rs56344012	0.05669
NM_002458.3(MUC5B):c.9010G>A (p.Ala3004Thr)	rs116870693	0.03214
NM_002458.3(MUC5B):c.11913T>C (p.Pro3971=)	rs367905040	0.02930
NM_002458.3(MUC5B):c.9181T>C (p.Ser3061Pro)	rs189329205	0.02674
NM_002458.3(MUC5B):c.9179A>C (p.Lys3060Thr)	rs184565965	0.02673
NM_002458.3(MUC5B):c.9140C>A (p.Thr3047Asn)	rs201236828	0.02641
NM_002458.3(MUC5B):c.13674T>C (p.Thr4558=)	rs202088302	0.02606
NM_002458.3(MUC5B):c.8900A>G (p.Asn2967Ser)	rs200811033	0.02553
NM_002458.3(MUC5B):c.7826T>C (p.Leu2609Pro)	rs2943496	0.02358
NM_002458.3(MUC5B):c.14718T>C (p.Pro4906=)	rs145066684	0.02192
NM_002458.3(MUC5B):c.8886T>C (p.Arg2962=)	rs368128605	0.02002
NM_002458.3(MUC5B):c.9143C>T (p.Ala3048Val)	rs188370271	0.01993
NM_002458.3(MUC5B):c.15826G>T (p.Val5276Leu)	rs55893724	0.00624
NM_002458.3(MUC5B):c.2429C>A (p.Thr810Asn)	rs190624357	0.00413
NM_002458.3(MUC5B):c.8709G>A (p.Ala2903=)	rs371299435	0.00147
NM_002458.3(MUC5B):c.1497C>T (p.Gly499=)	rs377351415	0.00146
NM_002458.3(MUC5B):c.16273G>A (p.Gly5425Arg)	rs201746407	0.00098
NM_002458.3(MUC5B):c.14584G>A (p.Gly4862Ser)	rs191989562	0.00073
NM_002458.3(MUC5B):c.17044G>A (p.Glu5682Lys)	rs200719329	0.00067
NM_002458.3(MUC5B):c.3846C>T (p.Gly1282=)	rs141821939	0.00066
NM_002458.3(MUC5B):c.3483T>C (p.His1161=)	rs376955587	0.00031
NM_002458.3(MUC5B):c.3926C>T (p.Thr1309Met)	rs200226020	0.00030
NM_002458.3(MUC5B):c.3584-10C>T	rs140245340	0.00025
NM_002458.3(MUC5B):c.200-12C>T	rs776408111	0.00006
NM_002458.3(MUC5B):c.15238G>A (p.Gly5080Ser)	rs200503009	0.00003
NM_002458.3(MUC5B):c.2478+8C>A	rs369614780	0.00003
NM_002458.3(MUC5B):c.14484A>G (p.Thr4828=)	rs199583764	0.00002
NM_002458.3(MUC5B):c.2925G>A (p.Ala975=)	rs551502589	0.00002
NM_002458.3(MUC5B):c.13124C>T (p.Ala4375Val)	rs201748966
NM_002458.3(MUC5B):c.13924A>G (p.Ile4642Val)	rs188444809
NM_002458.3(MUC5B):c.14491G>A (p.Ala4831Thr)	rs187205469
NM_002458.3(MUC5B):c.14586T>C (p.Gly4862=)	rs182667095
NM_002458.3(MUC5B):c.3198A>G (p.Ala1066=)	rs79118814
NM_002458.3(MUC5B):c.845C>A (p.Ala282Glu)	rs371465585

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