Most common CFTR mutations in the world

Name of MutationFrequency(%)Population with the highest prevalence
[[Delta]]F50828,948(66.0)
G542X1,062(2.4)Spanish
G551D717(1.6)English
N1303K589(1.3)Italian
W1282X536(1.2)Jewish-Askhenazi
R553X322(0.7)German
621+1G->T315(0.7)French-Canadian
1717-1G->A284(0.6)Italian
R117H133(0.3)
R1162X125(0.3)Italian
R347P106(0.2)
3849+10kbC->T104(0.2)
[[Delta]]I50793(0.2)
394delTT7810-30%*Nordic, Finnish
G85E67
R560T67
A455E62
1078delT57
2789+5G->A54Spanish
3659delC54
R334W53
1898+1G->T53
711+1G->T49French-Canadian
2183AA->G40Italian
3905insT386-17%*Swiss; Amish; Acadian
S549N30
2184delA29
Q359K/T360K87.5%*Jewish-Georgian
M1101K69%*Hutterite
Y122X48%*French, Reunion Island
1898+5G->T30%Chinese, Taiwan
3120+1G->A11%African-American
I148T9.1%French-Canadian

The source of data is obtained from the CF Genetic Analysis Consortium (1994). The frequency is based on the screening of 43,849 CF chromosomes, although not all of them have been tested for the indicated mutations. The mutations are found in patients of Caucasian origin, except indicated otherwise. The geographic location (or ethnic group) with the highest prevalence is indicated for some of the mutations. A rough relative frequency (expressed in %,*) is given for those mutations studied in relatively small-size samples or in the indicated populations only.