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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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Mutation Direct
Effortless mutation search and display tool
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Search criteria:
Gene:
TPR
& Disease:
CACP
, 4 results
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ClinVar
Gene
Nucleotide
Amino Acid
Transcript ID
Mutation type
Clinical Significance
Disease count
Publications
5655
TPR
c.*217_*218delinsCT
--
NM_003292.3
M
Indel
P
1
+
1
684665
TPR
c.*1657_*1674del
--
NM_003292.3
M
Del
P
1
+
1
684667
TPR
c.*1093G>C
--
NM_003292.3
M
SNV
P
1
+
1
1323494
TPR
c.*1130G>C
--
NM_003292.3
M
SNV
P
1
+
0
4 Results, 20 per Page
1
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