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ALS1
TP53
Amyotrophic Lateral Sclerosis 1
Lynch Syndrome
Cystic Fibrosis
COL4A5
Cowden Syndrome 1
Trp53
Dilated Cardiomyopathy
Phenylketonuria
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Variant Search
Amino acid Coordinates:--
AA:--
Codon:--
Clinvar ID
Nucleotide
Protein
Type
Clinical Significance
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Homo Sapiens
CFTR Variant
Change gene
Protein mutations
Genomic mutations
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CFTR Sequence
All
P: 0
LP: 0
LB: 0
B: 0
VUS: 0
#: mutation count; +: mutation count ≥ 99.
Genetic Comparison
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MW (kDa)
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* Relevance score in parentheses
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Diseases Comparison
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