ABCC7 p.Glu528*

ClinVar: c.1584G>A , p.Glu528= N , Benign
c.1584G>T , p.Glu528Asp ? , not provided
CF databases: c.1582G>A , p.Glu528Lys (CFTR1) ? , The mutation was identified in Polish child during CF newborn screening programme.

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[hide] Berkhout MC, van Rooden CJ, Rijntjes E, Fokkens WJ, el Bouazzaoui LH, Heijerman HG
Sinonasal manifestations of cystic fibrosis: a correlation between genotype and phenotype?
J Cyst Fibros. 2014 Jul;13(4):442-8. doi: 10.1016/j.jcf.2013.10.011. Epub 2013 Nov 5., [PMID:24210900]

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