This page contains an overview of the genetic variation in the CTF1 gene, including its role in inherited cardiac disease. For more details, click on the links below, or for a specific variant, enter the HGVS variant here:
Gene Name
cardiotrophin 1
Gene Links
Ensembl: ENSG00000150281 -
Locus Reference Genomic: LRG_408
Genomic Location
Chromosome 16 : 30,907,965 - 30,913,860 (forward strand)
View in: Ensembl -
UCSC Genome Browser
Canonical Seqs | Transcript (603 bases) | Protein (201 aa) |
---|---|---|
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ENST00000279804 | ENSP00000279804 |
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LRG_408t1 | LRG_408p1 |
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NM_001330.3 | |
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Q16619 |
VarType | DCM Freq | ExAC Freq | Case Excess |
---|---|---|---|
All | 0.00169 | 0.00046 | 0.12% |
Truncating | 0.00000 | 0.00006 | -0.01% |
Non-Truncating | 0.00169 | 0.00040 | 0.13% |
Details of the protein-altering CTF1 variants (missense, loss of function truncating, inframe indels and splice site regions) found in the ExAC database are shown below. To view lists of specific variants with links to detailed population frequency data, click on the variant numbers - for all or a particular variant class.
Total Variants | Combined frequency of rare variants | |
---|---|---|
All Variants | 20 | 0.00032 |
Truncating | 2 | 0.00003 |
Missense | 15 | 0.00020 |
Inframe | 0 | 0.00000 |
Splice Site | 3 | 0.00009 |