{{Rsnum
|rsid=121908812
|Chromosome=7
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=CFTR
|position=117592179
|Gene_s=CFTR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121908812
|Reversed=0
|FwdREF=T
|FwdALT=
|REF=AT
|ALT=A
|RSPOS=117232231
|CHROM=7
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002110200
|GENEINFO=CFTR:1080
|GENE_NAME=CFTR
|GENE_ID=1080
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.117232233delT
|CLNSRC=CFTR2; Cystic Fibrosis Mutation Database; GTR
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Cystic fibrosis
|Disease=Cystic fibrosis
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000029491.3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1250:C0010674:219700:586:190905008
|CLNSRCID=2143delT; 335; GTR000074114
}}{{PMID Auto
|PMID=1867536
|Title=Hepatic venous oxygen saturation monitoring in patients with assisted circulation for severe cardiac failure.
}}

{{PMID Auto
|PMID=2810954
|Title=The histological assessment and evaluation of a 4 day subrenal capsule assay by the percentage inhibition of DNA/protein.
}}

{{PMID Auto
|PMID=12007216
|Title=Cystic fibrosis: a worldwide analysis of CFTR mutations--correlation with incidence data and application to screening.
}}

{{PMID Auto
|PMID=15371903
|Title=CFTR mutation distribution among U.S. Hispanic and African American individuals: evaluation in cystic fibrosis patient and carrier screening populations.
}}

{{PMID Auto
|PMID=1283149
|Title=A termination mutation (2143delT) in the CFTR gene of German cystic fibrosis patients.
}}

{{PMID Auto
|PMID=9162681
|Title=[Detection of frequent mutations of the CFTR gene in cystic fibrosis patients from Central Russia].
}}

{{PMID Auto
|PMID=9272157
|Title=Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens.
}}

{{PMID Auto
|PMID=16051530
|Title=Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations.
}}
{{omim
|id=602421
|rsnum=121908812
}}