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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
Amyotrophic Lateral Sclerosis 1
USH2A c.8559-2A>G
Cystic Fibrosis
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Amino acid Site:--
AA:--
Codon:--
Clinvar ID
Codon
Nucleotide
Protein
Type
Clinical Significance
AI Predictor
Human
PIK3CD Variant
Genomic mutations
Protein mutations
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PIK3CD Sequence
All
P: 0
LP: 0
LB: 0
B: 0
VUS: 0
Variant of Interest
Second base in codon
First base in codon
Last base in codon
Position:
--
Codon Chart
CDS position:
--
Genomic location:
--
Region:
--
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